Enhancers that have rs10850635[chr12:116879887]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr12 116878888 116889024 enh47627

Transcript factors that have rs10850635[chr12:116879887]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr12 116877785 116882461 ZNF143 GTRD no Epithelial (MCF-7) 108061598
chr12 116877785 116882461 ZNF143 GTRD no Epithelial (MCF-7) 108061599
chr12 116878189 116879996 TCF7L2 GTRD no Colon (HCT116) 21577006
chr12 116878189 116879996 TCF7L2 GTRD no Colon (HCT116) 108061603
chr12 116878190 116880297 ZNF274 GTRD no Cervix (HeLa-S3) 108061604
chr12 116878272 116880234 ZNF274 GTRD no Cervix (HeLa-S3) 108061606
chr12 116878300 116880349 ZNF274 GTRD no Cervix (HeLa-S3) 108061607
chr12 116878368 116881241 ZNF143 GTRD no Epithelial (MCF-7) 108061609
chr12 116878434 116882122 ZBTB33 GTRD no Lung (A549) 108061615
chr12 116878452 116880631 TCF7L2 GTRD no Colon (HCT116) 21577010
chr12 116878452 116880631 TCF7L2 GTRD no Colon (HCT116) 108061617
chr12 116878490 116880171 TCF7L2 GTRD no Colon (HCT116) 21577012
chr12 116878490 116880171 TCF7L2 GTRD no Colon (HCT116) 108061624
chr12 116878628 116880144 ZNF274 GTRD no Bone Marrow (K562) 108061628
chr12 116878664 116879912 TCF7L2 GTRD no Colon (HCT116) 21577014
chr12 116878664 116879912 TCF7L2 GTRD no Colon (HCT116) 108061629
chr12 116879320 116880086 TCF7L2 GTRD no Colon (HCT116) 21577017
chr12 116879320 116880086 TCF7L2 GTRD no Colon (HCT116) 108061633
chr12 116879343 116880153 ZNF143 GTRD no Epithelial (MCF-7) 108061634
chr12 116879357 116880104 TCF7L2 GTRD no Colon (HCT116) 21577018
chr12 116879371 116880046 TCF7L2 GTRD no Colon (HCT116) 21577019
chr12 116879401 116881784 TCF7L2 GTRD no Colon (HCT116) 21577020
chr12 116879434 116880141 TCF7L2 GTRD no Colon (HCT116) 21577021
chr12 116879504 116880096 TCF7L2 GTRD no Colon (HCT116) 21577022
chr12 116879552 116880042 TCF7L2 GTRD no Colon (HCT116) 21577023
chr12 116879871 116879888 ESR1 JASPAR yes 123995807
chr12 116879871 116879889 ESR2 JASPAR yes 123995808

Genes associated with rs10850635[chr12:116879887], comfirmed by eQTL
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Blank TSI value indicates lack of sufficient expression for calculation
Chrom. Start End Strand Gene name Ensembl ID TSS of gene Distance between TSS and SNP Tissue q Value id More