Tag | Content |
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EnhancerAtlas ID | HS145-12065 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr2:9941220-9942450 |
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 | AATGAGGGCA AAGCGGCAGC CTGCAGTCGG ACAGCAGTGC TGGGTCCAGG GGCTCCTCAG 60 CTCCCACGCC CACTCACAGC GCATTGTCTC CAGGGGAAGG GTTTCTGGGC GGGCCCAGGA 120 AATGGGGATG TGTCATCCGA GTGGGTGCTC AGTCCCCAGC AGAGCTCACG GCTGACAGCC 180 AGGCCCGTCT CTCCTGTCAC TAGATCCCAC CTGCAGGGAC TTGCCCAGAG CTGACCTAAA 240 TTTCCCGGCC ACTCTGTCGA CACCTCCAGG GCGGGGCAAG GCATGCCTTC GCAGAAGCCC 300 AAACAGAATT CGTGACCAAC AGCACAGAGA CTCAACCTCC ACCCTGGGCT CAAAGGGCTG 360 CTGTGGTGGG CTTCCTGGGC ACTGCCTGAC CCTGAGCTCT CCCGGAAGCT GGCCTCTCAG 420 TGGGTGGGGG CAGACAGCAC CCGGGGAGGA TGTAGAAACA TGGCAGACAT GGGGATCTAG 480 GGCAGAGGGT GCCGTGTGTG TGTTCGAGGC CCGTTTCCTC TTTGTGAGTC TTCCAGTTTG 540 CTTTTCAGGG AAATAGACTC ATTTCAGACC CAGGAGAAAC GGTGGGCTTC AGCAGGGCTG 600 CCCCGGGGCC CACCTCCCGG AGCCTTGCTC CCTGCTTCAT CCAGGCACCT GGCTCTCCTG 660 CTGCCCTGGG GAAGTCAGAG CCTCCTATCT TGGCAGAAGC CCCCACCCCC AACCTCCGCA 720 CACTCAGTTC TCTTGCCACA CAGCCTAGAA AATTCTGCCT CTGGCTTGGG GCTCCATTTG 780 CTGAGCCAAG ATGAGGCATG AATCACAGGG CTGCGAGCTG CCTGAGGCTG TCTGGAACCC 840 GCAGACCTCA GAGCCCGCAG AACTGCAGCC CCTTCCCCCA CCACATCCCT GGGCCATGTC 900 GTCGCCGGCT TCTCGGCTCT TCTCTCACTG AGCCTGCCGT AGTTAAAACA GTTCCAACCT 960 CAAGGCAGCT CAGGTCTTGG GAGCCCAGAC AGCTCCTGGG GGTTTGTCGG CCTGATCAGA 1020 ATAAGCAAAT AGTATTCTTT TTAGATTTAT TTTCTTGGAT TACAAACTCA CAATTAAGTC 1080 TTTCTAGGCC GGGCGTGGTG ACTCATGCCT GTAATCCCAG CACTTTGGGA GGCCAAGGCG 1140 GGCGGATCAC TTGAGGTCAG GAGTTCGAAA GCAGCCTGAC CAACATAGTG AAACCCTGAC 1200 TCTACTGAAA ATACAAAAAT TAGCTGGGCA 1230
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