Enhancers that have rs8058997[chr16:2927005]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr16 2922182 2928184 enh86202

Transcript factors that have rs8058997[chr16:2927005]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr16 2926721 2927747 CTCF GTRD no Spleen 21685293
chr16 2926733 2927860 ZNF274 GTRD no Cervix (HeLa-S3) 21685294
chr16 2926782 2927606 TCF7L2 GTRD no Colon (HCT116) 21685295
chr16 2926847 2927549 ZNF274 GTRD no Cervix (HeLa-S3) 21685296
chr16 2926921 2927410 TCF7L2 GTRD no Colon (HCT116) 21685297
chr16 2926924 2927462 ZNF274 GTRD no Cervix (HeLa-S3) 21685298
chr16 2926937 2927537 ZNF274 GTRD no Cervix (HeLa-S3) 21685299
chr16 2926943 2927503 ZNF274 GTRD no Cervix (HeLa-S3) 21685300
chr16 2926953 2927304 TCF7L2 GTRD no Colon (HCT116) 21685301
chr16 2926998 2927363 TCF7L2 GTRD no Colon (HCT116) 21685302

Genes associated with rs8058997[chr16:2927005], 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