Enhancers that have rs184764156[chr11:72238438]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr11 72237585 72241735 enh110745

Transcript factors that have rs184764156[chr11:72238438]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr11 72237116 72238709 ZNF274 GTRD no Cervix (HeLa-S3) 21501678
chr11 72237263 72239156 ZNF274 GTRD no Cervix (HeLa-S3) 21501679
chr11 72237409 72239156 ZNF274 GTRD no Cervix (HeLa-S3) 21501680
chr11 72237802 72238942 ZNF274 GTRD no Cervix (HeLa-S3) 21501681
chr11 72238030 72238605 ZNF274 GTRD no Cervix (HeLa-S3) 21501682
chr11 72238032 72238651 ZNF274 GTRD no Cervix (HeLa-S3) 21501683
chr11 72238042 72238472 ZNF274 GTRD no Cervix (HeLa-S3) 21501684
chr11 72238093 72238600 ZNF274 GTRD no Cervix (HeLa-S3) 21501685
chr11 72238181 72238910 ZNF274 GTRD no Cervix (HeLa-S3) 21501686
chr11 72238426 72238444 NFYA JASPAR yes 39690371
chr11 72238429 72238438 VENTX JASPAR yes 39690372
chr11 72238429 72238439 ALX3 JASPAR yes 39690373
chr11 72238429 72238439 ESX1 JASPAR yes 39690374
chr11 72238429 72238439 GBX1 JASPAR yes 39690375
chr11 72238429 72238439 GBX2 JASPAR yes 39690376
chr11 72238429 72238439 GSX1 JASPAR yes 39690377
chr11 72238429 72238439 GSX2 JASPAR yes 39690378
chr11 72238429 72238439 HESX1 JASPAR yes 39690379
chr11 72238429 72238439 HOXB3 JASPAR yes 39690380
chr11 72238429 72238439 LBX2 JASPAR yes 39690381
chr11 72238429 72238439 LHX2 JASPAR yes 39690382
chr11 72238429 72238439 MIXL1 JASPAR yes 39690383
chr11 72238429 72238439 RAX JASPAR yes 39690384
chr11 72238430 72238438 BARX1 JASPAR yes 39690388
chr11 72238430 72238438 BSX JASPAR yes 39690389
chr11 72238430 72238438 EN1 JASPAR yes 39690390
chr11 72238430 72238438 ISX JASPAR yes 39690391
chr11 72238430 72238438 LHX9 JASPAR yes 39690392
chr11 72238430 72238438 MSX1 JASPAR yes 39690393
chr11 72238430 72238438 MSX2 JASPAR yes 39690394
chr11 72238430 72238438 PRRX1 JASPAR yes 39690395
chr11 72238430 72238438 RAX2 JASPAR yes 39690396
chr11 72238430 72238438 SHOX JASPAR yes 39690397

Genes associated with rs184764156[chr11:72238438], 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