Tag | Content |
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EnhancerAtlas ID | HS116-15408 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr17:74410480-74411720 |
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) |
Sox3 | MA0514.1 | chr17:74411494-74411504 | CCTTTGTTTT | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65659 | chr17:74410140-74411765 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 74410505 | 74410883 | chr17 | 74410960 | 74411663 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I076414 | chr17 | 74410478 | 74410930 |
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Enhancer Sequence | CTGAAAACAG TTATACACAA GTAAATAGAG CACTAAGCTG GGTGGGGAGA CCAGAAACTG 60 AGTCCTGTCT GGATGGCGGT GGGGGAAGGC AGGAGGACCG GGGTTGCAGG GGAACTGCAC 120 ACCAGGGACA GCCCCCACGC CCTCACCCCT GACACCCTCT CTGATCTCAC AACGCAGACT 180 CTCAGGCTGG GCAATACAGT GCTGCTGCAT CACCGCCTGG AAACTCGGCT GCAGCTCGCC 240 AGCTTGCTGG AATGGCCTGG AGGCACAGCC TGCCCGAGGG ACAGAGAAAG GGGACTGAGT 300 CCAACTGCCT GCTAAGTGAG GGGGAAGGAC TGCAGAGCTT GGCCTGGCAG GGGGCCAGCG 360 GGCTGGTCTC TGCAGATGCT GCGGTGTTTG ATAAGCAATA TGTGCACTTG GCGGCAGGAG 420 CTGGGAGCCG AGGAGCCCAG CCCTGCACCC CTCTGTCTTG GCTCTGGGCT TGTCAACCTG 480 GCTTAAAAAA AGACAAGAAC AGCCCAGGCC TGGCTCCTGC ATTTGAAGGG AGGGGACAGA 540 TGGGCATCTT TAGGAGAAGG CCGCCTCCTT CCTCAAAAGT ATAAGTAGAA GGCAGAAAAG 600 TGATCAGCAT GATTCCATGT TCTGTTCTTG TCAGGCCTGA CTGGGTATCA CTACCTAACC 660 AGTGGCCCCG GACTGCTCCA TTTCAGATGC GACAGGCTGC GGTCCTGTGG CTGCCGGGCA 720 TCCCTGAGAA CAAGAAGGGA GTCGGCCAGC TGGCCAGGCA CAGAGCAAGT TCACAGCCTC 780 AACACCCCTC AGTGTCTGAT GCCATGTTAG TTCACGGAAT GAGGACCCAG GCTGCTAATC 840 ACACAAACTG ATCCTGACGG AGCCTGCCAG GAAAGAACCC CACGTGCACT GCCTCTCCCA 900 ACCCTATGAC CCCCACGAAG GAGGCACCAC TCTTGTTCTC ATTCCACAGG AGACTGGGTG 960 GCTTGGAGAA GTAAGTGAGC TGCCTAAGGT CACCCAAGTG CCAGGACTCC AGAGCCTTTG 1020 TTTTGCTCAC CTGCCCTTCC TCATTTGACC TGTCTGGTCT CCAAGCATGG CCCTTGCTAC 1080 ACCTGGACCA ATTGGAACCA TGCTGCCATT CAAGTGTGGC CCTGGGCCTG GCGAGGTGGC 1140 TCACACCTGT AATCCCAGCA CTTTGAGAGG GCAAGGCGGT TGGATCACTT GAGGTCAGGA 1200 GTTGCAGACC AGCCTGGCCA ACATGGTGAA ACCTGGTCTC 1240
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