Tag | Content |
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EnhancerAtlas ID | HS139-08326 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr10:133836320-133837760 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF2 | MA0051.1 | chr10:133837375-133837393 | AGAAAGTGAAACCCGTTC | + | 6.06 | Mafb | MA0117.2 | chr10:133836627-133836639 | AATATGCTGACG | + | 6.18 | Nr2f6(var.2) | MA0728.1 | chr10:133837606-133837621 | TGAACTCCTGACCTT | - | 6.04 | Zfx | MA0146.2 | chr10:133837629-133837643 | CCCGCCTCGGCCTC | + | 6.01 |
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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 |
GH10I132022 | chr10 | 133836367 | 133837304 |
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Enhancer Sequence | TGGCAGGGAC CTGTAATCCC AGCTACTCGG GAGGCTGAGG CAGGAGAATC CCTTGAACCC 60 GGGAGGCGGA CGTTGCAGTG AGCCAAGATC AAGCCACTGC ACTCCAGCCT GGGCAACAGT 120 TCGAGATTCC ACCTCAAAAA AATGAACTGT CTGCCAGTCA TGGTGGTGCA TACCTGTGAT 180 CCCAGCACTT TGGGAGGCCG TGGCTGGAGG ACCGGAGCTT AGGGGTTCAA GACCAGCCTG 240 GGCAACATAT GGAGACCCTG TCTCTAAAAA GAAATTGTCG TATCGAACAA AGTTCCTTAA 300 TATCTGGAAT ATGCTGACGC CTTTCTTCCT GGATCTATTC CTGAGAAGGT GGTCACTGAG 360 CTTCCTCTTC CGAGACAGCC TGGCGCTCTG GACGCTTGGC TTCCGCTCGC TGGCTCGCCG 420 ACGCCCTCTG CTGTCCACGG TTGGGAGACC TGAAAGTCGC AAGAGCGTGC CCGTGACAGG 480 AGGCTGTGCG CAAGAAGACG TTTACAGCCG TTTTATTTGT AATAGCCCCA AACTGGAAAG 540 CAGACGGGTG TCCTTCAACA GGAGAATAGA TACATACACC GTGGCAAATT TGTACAAGAG 600 AACAATCTCC AGCAATAAAT AAGAGCACGC CACTGATGCG CGTGGCAATT TGGAAACCTT 660 CCACAGAACA GCACACGGAT TGCATGGATG CGAAGCTCCC CTCAACTAAT CTATGGGGAA 720 AATCATCAGA AAAAATGGGT GCCTCTGGGA GAGTAAGGGC AGGGACTAGC CAGAAGGGGC 780 AGCAGGGCCA GGTGGAGACT CACTCGCCTC TGTGGATACT CTGGTCATGC GGCTTGGGGA 840 GTGCGTGTCC CTTGAAGAGC CTGATCCAGA AACAGTGCCG TGTTTTCTGA AACTGAATGC 900 AACGAAGTGC GGCTTCATCC ACTGAGTCAC TGCCCATCCC CTCAAGGATC CCCAAGGAGG 960 CGACGCTGAG TCCGGAACGC AGGAGGGAGA CCGTTCTTCT TCCCGTGAGG AACATGCTCC 1020 AGGGTCCGGA GTCTACGGAA AAATAGGAGG GTTTGAGAAA GTGAAACCCG TTCATTTTCT 1080 GTGGAGCAGA ATCAGCAAAT GCTGTCTCGG GGGGCCCTGT GGGCCTTGGG AAGCATTTTG 1140 GACTAAACCA GAGGATAATG AGACACCACT GGAGGTTTAC CAGCAGAGGC GGTGCCATGG 1200 GGTTTGCGTC TCTAGAAGAT TCTATGGGGG ATCACCAGCA CGCCCAGCTA ATTTTTGTAT 1260 TTTTAGTACG TTGGCCAGGC TGGTCTTGAA CTCCTGACCT TCTGATCCAC CCGCCTCGGC 1320 CTCCCAAAGT GCTGGGATTA CAGGCGTGAG CCACCATGCC TGGTCCAAGT TTTGTATTTT 1380 TAGTAGAGAC AGGGTTTCAC CATGTTGGCC AGGCTGGTCT CGAACTCCTG ATCTCATGAT 1440
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