EnhancerDB
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  3. rs737629[chr17:74965412]
Enhancers that have rs737629[chr17:74965412]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr17 74962515 74968659 enh4612
Colon (HCT116) Blood (Karpas-422) Embryonic Stem Cell Line (H1-hESC)
Transcript factors that have rs737629[chr17:74965412]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr17 74961468 74965700 TCF7L2 GTRD no Colon (HCT116) 21789177
chr17 74961647 74965483 TCF7L2 GTRD no Colon (HCT116) 21789178
chr17 74961654 74965625 TCF7L2 GTRD no Colon (HCT116) 21789179
chr17 74962786 74965508 TCF7L2 GTRD no Colon (HCT116) 21789181
chr17 74964917 74965506 TCF7L2 GTRD no Colon (HCT116) 21789187
chr17 74965176 74965846 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 21789192
chr17 74965229 74965743 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 21789193
chr17 74965314 74965549 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 21789194
chr17 74965383 74965873 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 21789195
chr17 74965394 74965974 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 21789196
Genes associated with rs737629[chr17:74965412], 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