Tag | Content |
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EnhancerAtlas ID | HS002-05069 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr2:9940980-9942430 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr2:9942316-9942327 | GGTGACTCATG | + | 6.62 | JUND | MA0491.1 | chr2:9942316-9942327 | GGTGACTCATG | + | 6.02 | SP8 | MA0747.1 | chr2:9941282-9941294 | CCCACGCCCACT | + | 6.14 | TFAP2A | MA0003.3 | chr2:9942038-9942049 | TGCCTGAGGCT | - | 6.32 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_26755 | chr2:9937112-9944172 | Esophagus | SE_64906 | chr2:9939941-9943215 | NHEK |
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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 |
GH02I009797 | chr2 | 9937341 | 9944100 |
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Enhancer Sequence | TGTGTCTGTG CTGTGAACAT CCCAAGGGAC GGTGCAGCTG GTGGGGGTGG AGGGGCCGGA 60 GTGCTCTGAG GAGCCAGGGA AGGCCTCTCC GAGGAGGGGG CTTTTGAGCA GGAGGCCTGT 120 GCTTTGAGCA GAGATCCCAC AGAGGGTCCC AGGTCAGCTG GACCGGCACT TCAGAGAAGT 180 CACTGACTGA AGAATCAGAG GCAGGGGGCC CCACGAGCCG AGCCGGTCCA GGCCCCAGGG 240 AATGAGGGCA AAGCGGCAGC CTGCAGTCGG ACAGCAGTGC TGGGTCCAGG GGCTCCTCAG 300 CTCCCACGCC CACTCACAGC GCATTGTCTC CAGGGGAAGG GTTTCTGGGC GGGCCCAGGA 360 AATGGGGATG TGTCATCCGA GTGGGTGCTC AGTCCCCAGC AGAGCTCACG GCTGACAGCC 420 AGGCCCGTCT CTCCTGTCAC TAGATCCCAC CTGCAGGGAC TTGCCCAGAG CTGACCTAAA 480 TTTCCCGGCC ACTCTGTCGA CACCTCCAGG GCGGGGCAAG GCATGCCTTC GCAGAAGCCC 540 AAACAGAATT CGTGACCAAC AGCACAGAGA CTCAACCTCC ACCCTGGGCT CAAAGGGCTG 600 CTGTGGTGGG CTTCCTGGGC ACTGCCTGAC CCTGAGCTCT CCCGGAAGCT GGCCTCTCAG 660 TGGGTGGGGG CAGACAGCAC CCGGGGAGGA TGTAGAAACA TGGCAGACAT GGGGATCTAG 720 GGCAGAGGGT GCCGTGTGTG TGTTCGAGGC CCGTTTCCTC TTTGTGAGTC TTCCAGTTTG 780 CTTTTCAGGG AAATAGACTC ATTTCAGACC CAGGAGAAAC GGTGGGCTTC AGCAGGGCTG 840 CCCCGGGGCC CACCTCCCGG AGCCTTGCTC CCTGCTTCAT CCAGGCACCT GGCTCTCCTG 900 CTGCCCTGGG GAAGTCAGAG CCTCCTATCT TGGCAGAAGC CCCCACCCCC AACCTCCGCA 960 CACTCAGTTC TCTTGCCACA CAGCCTAGAA AATTCTGCCT CTGGCTTGGG GCTCCATTTG 1020 CTGAGCCAAG ATGAGGCATG AATCACAGGG CTGCGAGCTG CCTGAGGCTG TCTGGAACCC 1080 GCAGACCTCA GAGCCCGCAG AACTGCAGCC CCTTCCCCCA CCACATCCCT GGGCCATGTC 1140 GTCGCCGGCT TCTCGGCTCT TCTCTCACTG AGCCTGCCGT AGTTAAAACA GTTCCAACCT 1200 CAAGGCAGCT CAGGTCTTGG GAGCCCAGAC AGCTCCTGGG GGTTTGTCGG CCTGATCAGA 1260 ATAAGCAAAT AGTATTCTTT TTAGATTTAT TTTCTTGGAT TACAAACTCA CAATTAAGTC 1320 TTTCTAGGCC GGGCGTGGTG ACTCATGCCT GTAATCCCAG CACTTTGGGA GGCCAAGGCG 1380 GGCGGATCAC TTGAGGTCAG GAGTTCGAAA GCAGCCTGAC CAACATAGTG AAACCCTGAC 1440 TCTACTGAAA 1450
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