EnhancerDB
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  3. rs181617138[chr11:130016226]
Enhancers that have rs181617138[chr11:130016226]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr11 130012145 130023810 enh14400
Prostate (PC-3) Cervix (HeLa-S3) Blood (T-cell) Liver Blood (OCI-LY7) Blood (GM12878) Stomach Placenta Colon (HCT116) Peripheral Blood (MM.1S) Lung (PC-9) Pancreas Thymus Heart
Transcript factors that have rs181617138[chr11:130016226]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr11 130016137 130016717 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108008042
chr11 130016140 130016630 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108008043
chr11 130016150 130016583 CTCF UCSC Txn Factor no Conserved 108008044
chr11 130016160 130016760 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108008045
chr11 130016186 130016650 ZBTB33 ENCODE Uniform TFBS no Colon (HCT116) 21523793
chr11 130016186 130016650 ZBTB33 ENCODE Uniform TFBS no Colon (HCT116) 108008046
chr11 130016190 130016590 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 108008047
chr11 130016191 130016695 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21523794
chr11 130016191 130016695 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 108008048
chr11 130016213 130016228 STAT2 JASPAR yes 42417984
Genes associated with rs181617138[chr11:130016226], 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