Tag | Content |
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EnhancerAtlas ID | HS098-14772 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:122006780-122007960 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr12:122007713-122007734 | TCCTGCTTTCTTTTTTCTTTT | + | 6.14 | IRF1 | MA0050.2 | chr12:122007741-122007762 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | Myod1 | MA0499.1 | chr12:122007624-122007637 | AGCAGCTGTCCCT | + | 7.52 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_58854 | chr12:121951240-122029731 | Ly3 | SE_68743 | chr12:122006643-122007361 | H9 |
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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 |
GH12I121568 | chr12 | 122006219 | 122009070 |
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Enhancer Sequence | AAAAAAAAAA GGCTTGGAGC TGGGAACAGA CTGCTGATGG AGAAAAGCCC AATTTTAGGA 60 CATTAGAGAA GAGTCTGCAG CCCCGAGTTG TGTCCTGAAC ACCTGGTAGT GCACAAATCC 120 CTTTCTCAAA CGGCCACGTC CCGTGGTGCA GTGCCCAGGG CAAGGTAAGA CACTGGAAGA 180 CAGAGGCTGC AAGACACAGG CTGCGACCCC GCAATGACTG GGAGGGCTGG CCCAACCTTC 240 CCCACACACT GCCCTCCAAA GCAGACTCTC ACGTCTGTTA GGGCTGTGTT TATGTCACCC 300 AGCAACCCTG GAGAATCACT GCTTCCCCAC TTTCAGTCCA CGTGGTTCTG CTGGGCTGAC 360 CCCAGCCAGC AACTCCAGTC TGGCTGAAGG CTGTGCTAAG ACTGTCAGAG CCAATCCAGA 420 GGCATCTAAG GGAATGACTG AGGTTTTGGG AAGGACCCTG AGCTGGCAGG ATAGACGCCT 480 GAAGCTGCTG TGGGCCCCTT CTTCACCCAC CCTCCCTACC CTCCCATGGG GAGAAGCCTG 540 CCAAGAATGA AGCAGAAAGA GGGAGTCGAA GTGGGAAGCA GAAAGGAGAA ACAGACTCAA 600 TTTCTCAAGA TCATTTTGGA GCATCCAGAC ATAGATGTCC CCGGAGGTTA CATGCTGAAC 660 TTACGACCTA AGTCTATGAA TTTCCTTTTG CTTAGGACAG CTAGAGTTAC ATTTGTCACT 720 TAGGTCACTT ATAACAAATG TGCCCTATCA CCACTCTCTG GAAGCCTGTG TGCAGCTCAG 780 AGACCGAAAT GGGCATAATA ATTCCCCAGG CCAACTGCAG TCAGCGGCCT CCCTCAGAGT 840 TCAGAGCAGC TGTCCCTCTG CAAAGCACTT GAACATTCAT CGCTCCATTT GATCATCACA 900 GAAATACCAA GGGAGAGGGG GCTGGATGAC TGTTCCTGCT TTCTTTTTTC TTTTCTTTCT 960 TTCTTTCTTT CTTTTTTTTT TTGAGACAGG ATCTCGCTCT GTTGCCCTGA CAGAGTGGAG 1020 TGGAGTGCAG TGGCGTGATC TTGGCTCACT ACAGCCTCAA ACTCCTAGGC TCAAGTGATG 1080 TGTCCCACCT CAGCCTCCTG AGGAGCTGGG ACTACCGAGG CATGCCACCA AGCCCAGCTA 1140 ATTTTTGTGT TTTGGGTTTT TTGGGTTTTT TTGGTTTTGT 1180
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