Enhancers that have rs563742817[chr17:49022368]
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Transcript factors that have rs563742817[chr17:49022368]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr17 49021219 49023142 ZNF274 GTRD no Liver (HepG2) 21771448
chr17 49021483 49023420 ZNF274 GTRD no Cervix (HeLa-S3) 21771463
chr17 49021613 49022465 ZNF217 ENCODE Uniform TFBS no Epithelial (MCF-7) 21771470
chr17 49021924 49022380 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 21771518
chr17 49021937 49022401 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21771519
chr17 49021984 49022384 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 21771528
chr17 49022083 49023069 ZNF274 GTRD no Cervix (HeLa-S3) 21771553
chr17 49022086 49023021 ZNF274 GTRD no Cervix (HeLa-S3) 21771554
chr17 49022121 49023288 TCF7L2 GTRD no Colon (HCT116) 21771559
chr17 49022133 49023105 ZNF274 GTRD no Liver (HepG2) 21771560
chr17 49022151 49022473 ZNF274 GTRD no Bone Marrow (K562) 21771561
chr17 49022167 49022866 TCF7L2 GTRD no Colon (HCT116) 21771562
chr17 49022181 49022813 TCF7L2 GTRD no Colon (HCT116) 21771563
chr17 49022193 49023683 ZNF274 GTRD no Liver (HepG2) 21771564
chr17 49022222 49022760 TCF7L2 GTRD no Colon (HCT116) 21771565
chr17 49022245 49022775 ZBTB33 GTRD no Brain (SK-N-SH) 21771566
chr17 49022259 49023039 ZNF274 GTRD no Cervix (HeLa-S3) 21771567
chr17 49022287 49022737 TCF7L2 GTRD no Colon (HCT116) 21771568
chr17 49022290 49022916 TCF7L2 GTRD no Colon (HCT116) 21771569
chr17 49022298 49023001 ZNF143 GTRD no Epithelial (MCF-7) 21771570
chr17 49022302 49022696 ZNF143 GTRD no Epithelial (MCF-7) 21771571
chr17 49022311 49022899 ZNF143 GTRD no Epithelial (MCF-7) 21771572
chr17 49022325 49023040 ZNF274 GTRD no Liver (HepG2) 21771573
chr17 49022337 49022760 ZNF143 GTRD no Epithelial (MCF-7) 21771574
chr17 49022339 49023000 ZNF143 GTRD no Epithelial (MCF-7) 21771575
chr17 49022347 49022672 TCF7L2 GTRD no Colon (HCT116) 21771576
chr17 49022361 49022949 ZBTB33 GTRD no Brain (SK-N-SH) 21771577
chr17 49022367 49023393 ZNF274 GTRD no Bone Marrow (K562) 21771578

Genes associated with rs563742817[chr17:49022368], 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