EnhancerDB
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  3. rs117806933[chr16:69514862]
Enhancers that have rs117806933[chr16:69514862]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr16 69497735 69521555 enh16751
Bone Marrow (K562) Astrocyte Colon (HCT116) Uterus Epithelial (MCF-7) Stomach Skin (Keratinocyte) Bone (Osteoblast) Peripheral Blood (MM.1S) Pancreas (Panc1) Thymus Prostate (PC-3) Cervix (HeLa-S3) Esophagus Blood (GM12878) Placenta Lung (PC-9) Spleen Muscle (Myotube) Liver (HepG2) Prostate (RWPE1) Lung Heart
Transcript factors that have rs117806933[chr16:69514862]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr16 69513256 69514982 ZNF274 GTRD no Cervix (HeLa-S3) 21711882
chr16 69513761 69515844 ZNF274 GTRD no Cervix (HeLa-S3) 21711901
chr16 69514206 69514879 ZNF274 GTRD no Blood (GM12878) 21711907
chr16 69514570 69514954 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21711910
chr16 69514594 69514914 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21711911
chr16 69514621 69514961 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21711912
chr16 69514668 69516271 TCF7L2 GTRD no Colon (HCT116) 21711913
chr16 69514674 69514934 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 21711914
Genes associated with rs117806933[chr16:69514862], 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