Tag | Content |
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EnhancerAtlas ID | HS089-08606 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr22:30195850-30196970 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
STAT3 | MA0144.2 | chr22:30196646-30196657 | TTTCTGGGAAG | + | 6.02 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_00294 | chr22:30193866-30198657 | Adipose_Nuclei | SE_27345 | chr22:30193880-30196548 | Esophagus | SE_31847 | chr22:30194014-30196479 | Gastric | SE_31847 | chr22:30196516-30198578 | Gastric | SE_34183 | chr22:30191097-30197883 | HCC1954 | SE_42072 | chr22:30195964-30196443 | LNCaP | SE_51342 | chr22:30193849-30198654 | Skeletal_Muscle |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH22I029795 | chr22 | 30191424 | 30198522 |
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Enhancer Sequence | ATTGCAGCCT TGACCTCCTG GGCTTAAGTG ATCTTACTGC CTCAGCCTCC AGAGTAGCTG 60 GAACTATAGG CGTGTGCCAG CACACCCGGC TAATTTTTGT ATTTTTTGTA TATATGGGGT 120 TTCGCTATGT TGCCCAGGCT GGTCTCGAAC TCCTGGACTC AAGTGATCCA CCTGCCTTGG 180 CCTCCCAAAG TGCTGGGACT AGGCATGAGC CGCTGCACCC AGCCCTGATC TTTTCAAAAC 240 ATAAAATATG CTGGCTTTGT CGGTTCATGG GACCCTTTGC TGTGCTCACT ATGGCCTCGG 300 GACCACTGTC CCTGTTGCTC TGCTTGGGAA GCTTCTCCTT CCCTCCTTTG CAGAAGTGAC 360 CCCTCCTCAC CCTTTAGCTC TCGGTCCCAT GTCATGTTCT CAGAGGAGCC TTCTTGACTG 420 GGGTGAAGCC CTACCAAAGG CTCAGAATTC TGTGCACCTC CAGCTTGTAG TATTTGTTAT 480 ACCTGCAATT TGATGTTGCT TGTTTGATGA GTTGATTAAT GCAAACTCCA CGTGGGCAGG 540 GGCCGTGTCT GTTTCACTCC CCACTATATC CCCAGAACCT AATTAATCCA GAGCCTAGAA 600 TGCTGTAAGT ATTAGACAAA TATTTGTTGA ATAAATGGAT AAATCATGAA CGGAATTTTC 660 AATGCCAAAA AAGTAGGAAG GACATAAACT AAAAATAAAT AGAAAGGCCT TAAAGTGGAA 720 TATGTTCACC TTCTGAAAAG CTCATTCAAA GTCCTTAATT TTCTCACAGC CTGGGGAAAA 780 TCAGGTCAAA GAGTGGTTTC TGGGAAGCAC TGTCCACCAG TGATTTGATG GTTAACACAT 840 TAAAAGATGT AAGAAGAAGG GAAGAGGGGG ATAGTTTTGG CCCTTCTGGC CTTTTGCTAT 900 CAACAGGGGG GATTCACTAA CAGCCTCCCT GCACAGAGTC AGAACCTGAA GCCTGATCAG 960 TAGAGAACCT GCTCCTAACC ACTGGGGGTG CACAGGTCTA GGGTTGTGAA GGGATCCCTG 1020 TGCTGATACT CCATGGCCAA TTCTGCGAAG ATGGAGCCCT TGGTTTCCCT GTGTCCTCTC 1080 TGCACTTCCA GAGTTGGGGT ATCGGAACCC CATGGCCCAC 1120
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