Sample ID | Biosample type | Tissue type | Biosample name | TF Frequency |
---|---|---|---|---|
Sample_02_069 | Cell line | Brain | SF268 | 0.10687022900763 |
Sample_02_080 | Cell line | Lung | Calu-3 | 0.18181818181818 |
Sample_02_179 | Cell line | Urinary bladder | T24 | 0.14942528735632 |
Sample_02_317 | Cell line | Neuroblastoma | GICAN | 0.10810810810811 |
Sample ID | Tissue type | Biosample type | Biosample name |
---|
rsID | Chr | Start | Stop | Ref | Alt | Gene_region | Gene_symble | Effect | TCGA_Occurrence |
---|---|---|---|---|---|---|---|---|---|
rs765735196 | chr16 | 86601494 | 86601494 | G | A | exonic | FOXC2 | nonsynonymous | PAAD|1|185|0.00541 |
- | chr16 | 86602228 | 86602228 | C | T | exonic | FOXC2 | synonymous | ESCA|1|185|0.00541 |
- | chr16 | 86602427 | 86602427 | T | C | exonic | FOXC2 | nonsynonymous | LUSC|1|178|0.00562 |
- | chr16 | 86602380 | 86602380 | C | G | exonic | FOXC2 | nonsynonymous | PRAD|1|499|0.00200 |
- | chr16 | 86601231 | 86601231 | G | A | exonic | FOXC2 | nonsynonymous | PAAD|1|185|0.00541 |
rs148657129 | chr16 | 86602438 | 86602438 | G | A | exonic | FOXC2 | synonymous | COAD|1|367|0.00272,COADREAD|1|489|0.00204,SKCM|1|368|0.00272 |
- | chr16 | 86601058 | 86601058 | C | T | exonic | FOXC2 | synonymous | STAD|1|395|0.00253,STES|1|395|0.00253 |
- | chr16 | 86602418 | 86602418 | C | A | exonic | FOXC2 | nonsynonymous | LUAD|1|543|0.00184 |
- | chr16 | 86601995 | 86601995 | C | - | exonic | FOXC2 | frameshift | THCA|1|504|0.00198 |
rs773050488 | chr16 | 86601133 | 86601133 | C | T | exonic | FOXC2 | synonymous | UCEC|1|248|0.00403 |
rs778599000 | chr16 | 86602288 | 86602288 | C | T | exonic | FOXC2 | synonymous | STAD|1|395|0.00253,STES|1|395|0.00253 |
rs748779213 | chr16 | 86601025 | 86601025 | G | A | exonic | FOXC2 | synonymous | UCEC|1|248|0.00403 |
- | chr16 | 86602198 | 86602198 | G | A | exonic | FOXC2 | synonymous | PAAD|1|185|0.00541,PRAD|1|499|0.00200 |
- | chr16 | 86601138 | 86601138 | C | T | exonic | FOXC2 | nonsynonymous | PRAD|1|499|0.00200 |
- | chr16 | 86601098 | 86601098 | G | A | exonic | FOXC2 | nonsynonymous | LUSC|1|178|0.00562 |
- | chr16 | 86601239 | 86601239 | C | T | exonic | FOXC2 | stopgain | STAD|1|395|0.00253,STES|1|395|0.00253 |
- | chr16 | 86601261 | 86601261 | C | A | exonic | FOXC2 | nonsynonymous | OV|1|469|0.00213 |
rs138612549 | chr16 | 86602305 | 86602305 | A | G | exonic | FOXC2 | nonsynonymous | ACC|1|90|0.01111 |
- | chr16 | 86601490 | 86601490 | C | G | exonic | FOXC2 | synonymous | HNSC|1|512|0.00195 |
- | chr16 | 86602407 | 86602407 | G | T | exonic | FOXC2 | nonsynonymous | LIHC|1|373|0.00268 |
- | chr16 | 86601209 | 86601209 | G | A | exonic | FOXC2 | nonsynonymous | STAD|1|395|0.00253,STES|1|395|0.00253 |
- | chr16 | 86601563 | 86601563 | G | A | exonic | FOXC2 | nonsynonymous | BLCA|1|396|0.00253 |
- | chr16 | 86601093 | 86601093 | G | T | exonic | FOXC2 | nonsynonymous | LUAD|1|543|0.00184 |
- | chr16 | 86601175 | 86601175 | C | G | exonic | FOXC2 | nonsynonymous | LUAD|1|543|0.00184 |
rs773245007 | chr16 | 86602418 | 86602418 | C | T | exonic | FOXC2 | nonsynonymous | SKCM|1|368|0.00272 |
- | chr16 | 86601001 | 86601001 | C | T | exonic | FOXC2 | synonymous | COAD|1|367|0.00272,COADREAD|1|489|0.00204 |
- | chr16 | 86601502 | 86601502 | C | T | exonic | FOXC2 | synonymous | SKCM|1|368|0.00272 |
rs764129123 | chr16 | 86601062 | 86601062 | T | C | exonic | FOXC2 | nonsynonymous | LUAD|1|543|0.00184 |
- | chr16 | 86602184 | 86602184 | G | A | exonic | FOXC2 | nonsynonymous | SKCM|1|368|0.00272 |
- | chr16 | 86601425 | 86601425 | C | A | exonic | FOXC2 | nonsynonymous | LUAD|1|543|0.00184 |
- | chr16 | 86601105 | 86601105 | C | G | exonic | FOXC2 | nonsynonymous | BLCA|1|396|0.00253 |
rs764783770 | chr16 | 86602381 | 86602381 | C | T | exonic | FOXC2 | synonymous | SKCM|1|368|0.00272 |
- | chr16 | 86601397 | 86601397 | C | A | exonic | FOXC2 | synonymous | HNSC|1|512|0.00195 |
- | chr16 | 86601503 | 86601503 | C | T | exonic | FOXC2 | nonsynonymous | SKCM|2|368|0.00543 |
- | chr16 | 86600952 | 86600952 | G | A | exonic | FOXC2 | nonsynonymous | GBMLGG|1|820|0.00122,LGG|1|530|0.00189 |
- | chr16 | 86601010 | 86601010 | T | G | exonic | FOXC2 | nonsynonymous | KIPAN|1|799|0.00125,KIRP|1|282|0.00355 |
- | chr16 | 86601069 | 86601069 | G | A | exonic | FOXC2 | nonsynonymous | KIPAN|1|799|0.00125,KIRC|1|451|0.00222 |
- | chr16 | 86601394 | 86601394 | C | A | exonic | FOXC2 | nonsynonymous | LUSC|1|178|0.00562 |
- | chr16 | 86602406 | 86602406 | C | T | exonic | FOXC2 | nonsynonymous | SKCM|1|368|0.00272 |
- | chr16 | 86602312 | 86602312 | C | T | exonic | FOXC2 | synonymous | LUSC|1|178|0.00562 |
- | chr16 | 86601202 | 86601202 | C | A | exonic | FOXC2 | nonsynonymous | LUAD|1|543|0.00184 |
- | chr16 | 86601457 | 86601457 | C | T | exonic | FOXC2 | synonymous | UCEC|1|248|0.00403 |
- | chr16 | 86601304 | 86601304 | C | A | exonic | FOXC2 | synonymous | LUAD|1|543|0.00184 |
- | chr16 | 86602295 | 86602295 | G | A | exonic | FOXC2 | nonsynonymous | CESC|1|194|0.00515 |
- | chr16 | 86601059 | 86601059 | G | A | exonic | FOXC2 | nonsynonymous | COAD|1|367|0.00272,COADREAD|1|489|0.00204 |
rs755617186 | chr16 | 86601967 | 86601967 | C | T | exonic | FOXC2 | synonymous | STAD|1|395|0.00253,STES|1|395|0.00253 |
- | chr16 | 86601383 | 86601383 | C | A | exonic | FOXC2 | nonsynonymous | PAAD|1|185|0.00541 |
- | chr16 | 86600960 | 86600960 | G | A | exonic | FOXC2 | nonsynonymous | HNSC|1|512|0.00195 |
- | chr16 | 86601483 | 86601483 | C | G | exonic | FOXC2 | nonsynonymous | LUAD|1|543|0.00184 |
- | chr16 | 86601603 | 86601603 | C | T | exonic | FOXC2 | nonsynonymous | STAD|1|395|0.00253,STES|1|395|0.00253 |
- | chr16 | 86601141 | 86601141 | C | A | exonic | FOXC2 | nonsynonymous | PAAD|1|185|0.00541 |
rs759417459 | chr16 | 86601223 | 86601223 | C | T | exonic | FOXC2 | synonymous | STAD|1|395|0.00253,STES|1|395|0.00253 |
- | chr16 | 86601350 | 86601350 | G | A | exonic | FOXC2 | nonsynonymous | STAD|1|395|0.00253,STES|1|395|0.00253 |
- | chr16 | 86601011 | 86601011 | T | C | exonic | FOXC2 | nonsynonymous | STAD|1|395|0.00253,STES|1|395|0.00253 |
- | chr16 | 86601196 | 86601196 | C | A | exonic | FOXC2 | synonymous | ACC|1|90|0.01111 |
- | chr16 | 86601361 | 86601361 | C | T | exonic | FOXC2 | synonymous | UCEC|1|248|0.00403 |
- | chr16 | 86602395 | 86602395 | C | A | exonic | FOXC2 | nonsynonymous | HNSC|1|512|0.00195 |
- | chr16 | 86602257 | 86602257 | C | G | exonic | FOXC2 | nonsynonymous | STAD|2|395|0.00506,STES|2|395|0.00506 |
- | chr16 | 86601587 | 86601587 | G | A | exonic | FOXC2 | nonsynonymous | HNSC|1|512|0.00195,SKCM|2|368|0.00543 |
- | chr16 | 86602192 | 86602192 | C | G | exonic | FOXC2 | synonymous | LUAD|2|543|0.00368 |
- | chr16 | 86601500 | 86601500 | C | - | exonic | FOXC2 | frameshift | STAD|1|395|0.00253,STES|1|395|0.00253 |
- | chr16 | 86601557 | 86601557 | G | C | exonic | FOXC2 | nonsynonymous | LUAD|1|543|0.00184 |
- | chr16 | 86601305 | 86601305 | C | A | exonic | FOXC2 | nonsynonymous | LUAD|1|543|0.00184 |
- | chr16 | 86601425 | 86601425 | C | T | exonic | FOXC2 | synonymous | BLCA|1|396|0.00253 |
- | chr16 | 86601480 | 86601480 | G | - | exonic | FOXC2 | frameshift | SKCM|1|368|0.00272 |
- | chr16 | 86601790 | 86601790 | G | - | exonic | FOXC2 | frameshift | BLCA|1|396|0.00253 |
rs751774927 | chr16 | 86601504 | 86601504 | C | T | exonic | FOXC2 | nonsynonymous | BLCA|1|396|0.00253,HNSC|1|512|0.00195 |
TF_name | Disease_name | Disease_class | Disease_semantic_type | TF_disease_source |
---|---|---|---|---|
FOXC2 | Hydrops Fetalis | C13;C15;C16;C20;C23 | Disease or Syndrome | GENOMICS_ENGLAND |
FOXC2 | Lymphatic Diseases | C15 | Disease or Syndrome | GENOMICS_ENGLAND |
FOXC2 | Tetralogy of Fallot | C14;C16 | Congenital Abnormality | CTD_human |
FOXC2 | Congenital musculoskeletal anomalies | C05;C16 | Congenital Abnormality | CTD_human |
FOXC2 | Congenital diaphragmatic hernia | C16;C23 | Disease or Syndrome | CTD_human |
FOXC2 | Cardiovascular Abnormalities | C14;C16 | Congenital Abnormality | CTD_human |
FOXC2 | Lymphedema distichiasis syndrome | C15 | Disease or Syndrome | CTD_human;ORPHANET;UNIPROT |
FOXC2 | Congenital hernia of foramen of Morgagni | C16;C23 | Congenital Abnormality | CTD_human |
FOXC2 | Congenital hernia of foramen of Bochdalek | C16;C23 | Congenital Abnormality | CTD_human |
FOXC2 | Craniofacial Abnormalities | C05;C16 | Congenital Abnormality | CTD_human |
FOXC2 | Cakut | C12;C13;C16 | Disease or Syndrome | GENOMICS_ENGLAND |
FOXC2 | Lymphedema-Distichiasis Syndrome with Renal Disease and Diabetes Mellitus | C12;C13;C15;C18;C19 | Disease or Syndrome | UNIPROT |
FOXC2 | Intellectual Disability | C10;C23;F01;F03 | Mental or Behavioral Dysfunction | GENOMICS_ENGLAND |
pathway_ID | pathway_name | pathway_source | gene_number | edge_number |
---|
GO_term_name | GO_term_type | TF_name |
---|---|---|
GO_RESPONSE_TO_NITROGEN_COMPOUND | BP | FOXC2 |
GO_METANEPHROS_DEVELOPMENT | BP | FOXC2 |
GO_COLLAGEN_FIBRIL_ORGANIZATION | BP | FOXC2 |
GO_EMBRYONIC_SKELETAL_SYSTEM_DEVELOPMENT | BP | FOXC2 |
GO_POSITIVE_REGULATION_OF_LOCOMOTION | BP | FOXC2 |
GO_VASCULAR_ENDOTHELIAL_GROWTH_FACTOR_RECEPTOR_SIGNALING_PATHWAY | BP | FOXC2 |
GO_MORPHOGENESIS_OF_AN_EPITHELIUM | BP | FOXC2 |
GO_KIDNEY_EPITHELIUM_DEVELOPMENT | BP | FOXC2 |
GO_MUSCLE_CELL_PROLIFERATION | BP | FOXC2 |
GO_EMBRYONIC_VISCEROCRANIUM_MORPHOGENESIS | BP | FOXC2 |
GO_PATTERNING_OF_BLOOD_VESSELS | BP | FOXC2 |
GO_EMBRYONIC_HEART_TUBE_DEVELOPMENT | BP | FOXC2 |
GO_ARTERY_MORPHOGENESIS | BP | FOXC2 |
GO_VENTRICULAR_CARDIAC_MUSCLE_TISSUE_DEVELOPMENT | BP | FOXC2 |
GO_MESENCHYMAL_CELL_DIFFERENTIATION | BP | FOXC2 |
GO_CELL_DIFFERENTIATION_INVOLVED_IN_KIDNEY_DEVELOPMENT | BP | FOXC2 |
GO_CELL_FATE_COMMITMENT_INVOLVED_IN_FORMATION_OF_PRIMARY_GERM_LAYER | BP | FOXC2 |
GO_ENZYME_LINKED_RECEPTOR_PROTEIN_SIGNALING_PATHWAY | BP | FOXC2 |
GO_REGULATION_OF_HEART_MORPHOGENESIS | BP | FOXC2 |
GO_NEPHRON_EPITHELIUM_DEVELOPMENT | BP | FOXC2 |
GO_LYMPHANGIOGENESIS | BP | FOXC2 |
GO_POSITIVE_REGULATION_OF_CELL_ADHESION | BP | FOXC2 |
GO_REGULATION_OF_CELL_MIGRATION_INVOLVED_IN_SPROUTING_ANGIOGENESIS | BP | FOXC2 |
GO_REGULATION_OF_CELL_ADHESION_MEDIATED_BY_INTEGRIN | BP | FOXC2 |
GO_GLOMERULUS_DEVELOPMENT | BP | FOXC2 |
GO_CARDIAC_MUSCLE_TISSUE_MORPHOGENESIS | BP | FOXC2 |
GO_MUSCLE_ORGAN_MORPHOGENESIS | BP | FOXC2 |
GO_POSITIVE_REGULATION_OF_CELL_ADHESION_MEDIATED_BY_INTEGRIN | BP | FOXC2 |
GO_ORGAN_GROWTH | BP | FOXC2 |
GO_MESODERM_MORPHOGENESIS | BP | FOXC2 |
GO_INSULIN_RECEPTOR_SIGNALING_PATHWAY | BP | FOXC2 |
GO_BLOOD_VESSEL_REMODELING | BP | FOXC2 |
GO_OSSIFICATION | BP | FOXC2 |
GO_MESODERMAL_CELL_DIFFERENTIATION | BP | FOXC2 |
GO_LYMPH_VESSEL_MORPHOGENESIS | BP | FOXC2 |
GO_GLOMERULAR_EPITHELIUM_DEVELOPMENT | BP | FOXC2 |
GO_POSITIVE_REGULATION_OF_WOUND_HEALING | BP | FOXC2 |
GO_RENAL_SYSTEM_VASCULATURE_DEVELOPMENT | BP | FOXC2 |
GO_MORPHOGENESIS_OF_A_BRANCHING_STRUCTURE | BP | FOXC2 |
GO_STRIATED_MUSCLE_CELL_PROLIFERATION | BP | FOXC2 |
GO_POSITIVE_REGULATION_OF_EPITHELIAL_CELL_MIGRATION | BP | FOXC2 |
GO_POSITIVE_REGULATION_OF_SPROUTING_ANGIOGENESIS | BP | FOXC2 |
GO_PARAXIAL_MESODERM_DEVELOPMENT | BP | FOXC2 |
GO_EPITHELIAL_CELL_DIFFERENTIATION_INVOLVED_IN_KIDNEY_DEVELOPMENT | BP | FOXC2 |
GO_HEART_GROWTH | BP | FOXC2 |
GO_TRANSMEMBRANE_RECEPTOR_PROTEIN_TYROSINE_KINASE_SIGNALING_PATHWAY | BP | FOXC2 |
GO_LYMPH_VESSEL_DEVELOPMENT | BP | FOXC2 |
GO_REGULATION_OF_SPROUTING_ANGIOGENESIS | BP | FOXC2 |
GO_NEPHRON_DEVELOPMENT | BP | FOXC2 |
GO_MESENCHYME_MORPHOGENESIS | BP | FOXC2 |
GO_SOMITE_DEVELOPMENT | BP | FOXC2 |
GO_REGULATION_OF_CELL_DEVELOPMENT | BP | FOXC2 |
GO_MESONEPHROS_DEVELOPMENT | BP | FOXC2 |
GO_MESODERMAL_CELL_FATE_COMMITMENT | BP | FOXC2 |
GO_REGIONALIZATION | BP | FOXC2 |
GO_POSITIVE_REGULATION_OF_BLOOD_VESSEL_ENDOTHELIAL_CELL_MIGRATION | BP | FOXC2 |
GO_NEURAL_CREST_CELL_DIFFERENTIATION | BP | FOXC2 |
GO_EMBRYONIC_CRANIAL_SKELETON_MORPHOGENESIS | BP | FOXC2 |
GO_TRANSCRIPTION_FACTOR_ACTIVITY_RNA_POLYMERASE_II_DISTAL_ENHANCER_SEQUENCE_SPECIFIC_BINDING | MF | FOXC2 |
GO_CHROMATIN_DNA_BINDING | MF | FOXC2 |