Tag | Content |
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EnhancerAtlas ID | HS116-32931 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr8:27975390-27976720 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr8:27976157-27976168 | CTGAGTCACCC | - | 6.02 | IRF1 | MA0050.2 | chr8:27976675-27976696 | TTTTACTTTCTCTTTTGGTCA | + | 6.26 | JUNB | MA0490.1 | chr8:27976157-27976168 | CTGAGTCACCC | - | 6.02 | KLF16 | MA0741.1 | chr8:27976395-27976406 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr8:27976395-27976405 | GCCCCGCCCC | + | 6.02 | SP3 | MA0746.2 | chr8:27976394-27976407 | CGCCCCGCCCCCC | + | 6.11 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I028116 | chr8 | 27973625 | 27977015 |
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Enhancer Sequence | CTAGAGACAG AAAGTATTTT CAAGTGTTGG CATAATTGTG AAATAAAAAG CAGCCCAGAG 60 AAGTTGTGGT TTTGACATAA TGTGGCCCTC GGAAATGTTT GGATTTGACC TTGCCCTTCT 120 CTCTCATCCT GCCCAGAGTC TATGAGTGAA AACTGGTTGG TTTGCACAGC GTAGCCCACT 180 GCTCTTAGAT GTAAGGTGAT GAACTTCATG TTTATTTTAC TTTTGTTTTT GCTTGCTGAC 240 TACATAGATG TAAACTGACT TTCATTAGCT TAGCAGGGTT TTTTAAAGAT TAATTTTAAA 300 TTAGGTTAAA AATGATGTAT TGTGACCTAT GAGTCAGCAA GCAGCATTTA AGGTTAATAG 360 TCTGTTCACG TTAGGGTCAA GTTTTACTGC TGTGTTGGCT CAGGTGTCCC TGCTATGTTT 420 TCATATGTTG AACCTGATTA AAGTTTTGCT TCTTAAAAGA ATAGGAGTTA AGGTAAAGAA 480 AAGCCCCAGC AAGCAGAGCC TGGTTATTAT TTATGGCAAG CTAGTAGCAA GCAGTGTGTT 540 ATATATATTC TCGTGGATGG ATAAATTGGA AAGTTGAGTG AACAGAGAGT TCAAGGACAA 600 AACAGGTATG GCTTTTGTGA AGGCTCATTA AATCAAGCAA AGTGCTAATC ACTCAGTACT 660 ATCAGCTGGA CTGAGATTCT TCAGTAGTCT CCAGAGAGCA ACAATTACTG GTGACTGTCA 720 TCGTGTAACA ATCAGGCTCT GGAGATGAAA AAGACCGGTA GTGGGATCTG AGTCACCCAT 780 TCACTAGAAT GCAAATGTTG CCAAATAACT CCAACAACCT TTTAAAATAG TTTTATTCCT 840 TTTTAATCAG CTTTGCCCAG AAGCAGTTTT ACATTCAATC TTTAATGCTC CTTGGCTGTT 900 TTCACAAGAT GCAATTTAAA GGGTAGTTAC CCATTAAAAA GTGAGTGAGT CATACTTTCT 960 CCCTGTGGAA TTTTAAATTC ATTTCCCGTT CCTTCCTCTT CCCCCGCCCC GCCCCCCACG 1020 CCCCATTAAT GACTTTAGAT CCTCCAACTA TGTTCTTACC TGTCTGAGAA AAGCTGAAGT 1080 GCTAGGTAAT GCTAGGTACC AGGCCCAGAA GACAATTTCG TAGACTTGCA CAGCTGCAAC 1140 GGAAGCAAAA GGAACCTACA GAGACCTGAG AGTGAGTGAC TGTGGCCCTG CTGCCCTGGG 1200 CGTCATTTCT GGCAGGCCTC AGGACCTTCT GCATTTCTGG GCTTTGACGC TGACACTGCT 1260 TATCTCTCAC TTTTTCTATT GACCATTTTA CTTTCTCTTT TGGTCACCCA GATTTCCATA 1320 CATGGTGACC 1330
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