Tag | Content |
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EnhancerAtlas ID | HS116-08129 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr12:42868700-42869400 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr12:42869066-42869087 | CATGGCTTTCTGTTTCATTTT | + | 6.72 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH12I042472 | chr12 | 42866017 | 42869522 |
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Enhancer Sequence | GATTATAAAA CAAGAGAAAA CATCACAAAT TAAGACAAGC CATGGATTTT CCAAGCCAGC 60 ACAAAGATAC AGATTGCCGA AGATGTGAAT TACTTTTACA GCTGTACTCC CTGATTAGCC 120 TTTTTGTGAA AAATGTGCAG TAAATTACTA TCCTAATCAA GGTAAATCAA CGTTAGCACT 180 ACATGCCACC ATCCCACCAT CCCCTCCTCC CAATCACCTG GAAGTTCTGG CCACATCTCA 240 ATCTTACAAT TCCCACAAGT TCATTCCAGC CTTTCAACAA ATTACACTGA GGATTGACTG 300 TCATTCATGC ACAAAGTAAA GAGTCCAACT GAAGGACATG AGTGACAATA CCCTTTTCAT 360 TACAGGCATG GCTTTCTGTT TCATTTTTTA GCAGATGGCT AACTTACTTC TCCATGCCTG 420 GCTGGTACCA TTAGTGTTAC GGCATTTAAT CACTGCATCA AGCAACCCAC GGTAAGTGGT 480 GTCTCATTTA ACAGATGGGG AAACTGGGCC TCAGAGCAAT GTCCCTCAGG GTCAATTGCC 540 CAAGGTCAGT AAGTGGTCTT AGGACCGGTC TTGGCTGTGA TCCTAAACCC CTGCAACCCC 600 ACACTGCCTC CAGGGGGGGA GTGCTGATGG AGCCAATTCC TTTTTCTTTG GTGAATCAGC 660 CAAGCTACCT GCGCTGCAGA CACACAAAAT GACACAACTG 700
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