Tag | Content |
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EnhancerAtlas ID | HS118-10193 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr2:101491860-101493340 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr2:101493064-101493075 | GGTGACTCATG | + | 6.62 | JUND | MA0491.1 | chr2:101493064-101493075 | GGTGACTCATG | + | 6.02 | MEF2A | MA0052.3 | chr2:101492446-101492458 | GCTATTTTTAGC | - | 6.44 | MEF2B | MA0660.1 | chr2:101492446-101492458 | GCTATTTTTAGC | - | 6.92 | MEF2C | MA0497.1 | chr2:101492445-101492460 | AGCTATTTTTAGCCT | - | 6.92 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_56097 | chr2:101492367-101495351 | u87 |
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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 |
GH02I100875 | chr2 | 101491618 | 101493618 |
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Enhancer Sequence | ATTTTTAATT ATATGTATTT TACCACAATT TTTAAAAATA AAATTTTTAA AAATTAAAAG 60 CTTACACACA CACACACACA CACACACACA CACACACACA CACACACAGC ATGTAGGGAT 120 CACACAGATG TGAGCATGAT GCCCCAGTGT TGGCATGAGA CAGTCGCTTT CCTTAGCTGG 180 TTCCTACACA GCGCGGCTCC TGGACGCGCA GCTTGTCGAG GCTTGAAAGG CGCGGGCAGG 240 GCTGCCTCCC CTTAGCTTTG TAGACCGAAG GTCGTTTACT TTGGCATTTT TAACAAAGAT 300 TTAAAGTTTC TGGAATTTGC CAGCCTGCTT GGTCCCGAGG CCCAGATTAA GCAGCATGCA 360 CTTTTTTCCT TAAACGCAGA ACAATGGCAG ACGGCATGAA AGCTTTCCCA GGGTTATTTT 420 TCCCTTGAAG TAACAAAAGG GGAGACGGAT GAGGAAAAAA CACCCACATG GAATCAAATA 480 CCGCAGAAAG CAAACTTCAA GCCACGTGAT ATTAGCACAG AAGGGAAATG GGAGGATGGG 540 TTAAAACCGT GTGAAGTGCT CAGAGTTCTG AAGTGAGGGC TCTTAAGCTA TTTTTAGCCT 600 CAAAAATGCT ATAAATCCTG TTATCCCATT ACACTCCAGT GGATCGAATT ATTTGCTTTT 660 CTCTACCTTT ACCACTCTAA TTTTTTTTTG TTTGAGTAAA TGAGAGCAGG CCTTCTCAGA 720 GGCAGCTGAC ATCAGACAGA GACTTCCTTT GCGGCCTCTC TGGTTCTGTT CCTCTCTTCC 780 CCGTAGCTGG TATTTGTAGT GACACCTGGG AGCCACAGAT TTGCTTAGCA ACCTTTCTCC 840 AGGGTGAACA GGGTATTCAC AACTCCTGAA CCAAGGCGTG TGGCTGGTAT CATTTTGTGG 900 GGCCAGAACG CATTGCGTGG AGAAATTCAG TGATGACCTG GTCCCCACGC CTGCTGCTCA 960 GGGCCCCATC ACCCTCGTGA CTGTCAGTGG TGCTGCTTCC CACGTCTCCT AAGAGGGCTT 1020 CAGGAGAACG TAGAACGAGG TATCTGTCTC TTCCTTTCGG ACCTGGCCTT TCCATTTGGC 1080 CATATGTCAG AATTTCCAGC TGCCCTAGGG GCCCAGGAAT CTGTATTTTA GTTGCTTTCC 1140 AAATAATTCT GCTGCCCAGC TGTATTTGGA GACTATAGCC TTAAATCAGT GATTCCCCGT 1200 CAGTGGTGAC TCATGAAGAG CTTAGATGTG GGCCTGGTGT GTGGTTGGTG GCAAGGGGAG 1260 TCTTTCAGAT CCCTTCTGCT TGTTGCTGTT GGTGGCAGGA GCGTGCATGT TATGGTGGCT 1320 CAGGCCTAAT CCCATCTGTT TGGGCATCTC GCCTGTCTGG AAAACAGGTC CCGGAGCCAT 1380 GCACACCAAG CTCCTAGGGA AGGCAGAGAG CACTCCCCGA CTCTTAACAA AGACATGTGG 1440 AGGTGGACGT CTGCCCTTAA GCACTCAGGG TTCAAGAAAT 1480
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