Tag | Content |
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EnhancerAtlas ID | HS064-03094 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr12:12693290-12694750 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr12:12694063-12694075 | TCTATTTTTAGT | - | 6.27 | MEF2B | MA0660.1 | chr12:12694063-12694075 | TCTATTTTTAGT | - | 6.32 | NKX2-3 | MA0672.1 | chr12:12693565-12693575 | TTCAAGTGGT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_27729 | chr12:12691562-12693971 | Fetal_Intestine |
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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 |
GH12I012538 | chr12 | 12691535 | 12693761 |
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Enhancer Sequence | AATTTTTAAA GATGGTATTT AACCAGAGTC AGGAGTTTTC GTAACATATT AACATCCAAT 60 ACAAGGAACA CTAGGTTAGA AAATGCTCAT TCAGCTATTT CCCTTGTACA GTGGGTCTAA 120 CTTGTGCTTC CTTCACTTAC ACAACAGTTT TTGAACATCT ATACTGTGCA AGGCTTTTTG 180 CTCAAGGAAT CTTTGGAGGA TACAATTTTA AAGCAATTTC ATAAGATATC TATAAGGCTC 240 CGTGAGATCA CATAGCAAGA GTGGGAGAGA AAAATTTCAA GTGGTGACAT CTAGAAGTCA 300 ACAGGAGGAG GTGAGGAGGT GGTCAATCCC ACCTATGTAT TTATTCTGGA CGCTCTCCTA 360 CCCCAACTCC TTAGGGTGCT ACACAATCTC TTTGTATTCA CAAATAACCC CTGGTCAAGA 420 GGTTTGGAGG GAGCGGCGAC ACCACCAGCC AGCAAACTTC TACTAATTCT GGAGGCAACT 480 TCCTGTCAGC TGGTCCCTAA AGGCTGGTTG CTTCCTGCCA GGAGGCCACT TAGCACAGAT 540 TCATCTTTCT TCAGGAGGCA GACAGTTGCT TTTTTTTCTT TTCTTTTCTT TTCTTTTTTT 600 TTTTTTTTTT TTTTTTTGAG CCAGGAGTCT CACTCTGATT GCCCAGGCTG GAGTGCAGTG 660 GTGCTGATCA TGGCTCACTG CAGCCTCAAC CTCCCAGGCT CAGGTGATCC CCCCAGCTCA 720 GCCTCCCGAG TAACTGGGAC TACATGTGCA CACCATCACG CCTGGCTAAT TTCTCTATTT 780 TTAGTAGAGC TGGAGTTTCA CCATGTTGCC CAGACTGGTC TCAAACTCCT GGACTCAAGC 840 AATTGACTCA CCTCAGTCTC CCAAAGTCCT GGGATTATGG GCGTGAGCCA CCGCACCTGG 900 CCACTTGCTG ATTCTCACTG TGGCACTGAT TTTAGAGGGA AAGGCAGAGG GGAAGACAAT 960 TCATCTTCCC TTCAACCCCA GGTACACACA GTCCCCTGCC CCACACAAAT ACAAACATGA 1020 AGAATAAAAG AGGTACAGGC CTTGACAAGG TTACACTGAC ATTATTTCCA CCCAACAGTA 1080 TCTCCCACAA AGCGTTAAGG AGGGAAAATA AGAAACTCTT ATTAAAATTA GTCTATCTTA 1140 TTGGAAGGCC CAGTAAGGTA GGTAAATGGC ATAAATTCTC AGGAGTTGGT CAATCTATGA 1200 TAGTTGTAGT TGGAATGAGC TGTCTGTCTA GACCCATGGT CTTCAAGCTT TTCAGCTGAC 1260 AGCCCACTTC AGAGTGACAA ACTACCAGGT CTATGTCTTC CTAACAACTA TTTCTCTGTC 1320 TACATGTGTT CCACCACAAA CCCTAGAGAG AAATAACTGT GAAAAAAATT CTGTAAAGTG 1380 AGATATAACA TCCAGATTAA AATGTAAATA CAAGAGCACT GAAAATGTAT GCACATGTAA 1440 CAAACCTGCA CATATACCCC 1460
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