Tag | Content |
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EnhancerAtlas ID | HS091-14586 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr15:42090580-42092020 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr15:42091593-42091608 | AGGTCAGAGTGGCCT | + | 6.66 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_27312 | chr15:42090762-42092287 | Esophagus | SE_28287 | chr15:42091009-42092175 | Fetal_Intestine | SE_35965 | chr15:42090630-42092312 | HMEC | SE_64247 | chr15:42090822-42092382 | 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 |
GH15I041798 | chr15 | 42090711 | 42092258 |
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Enhancer Sequence | AATGAATCTC ATGCCTCAGC CTCCTGATTA GCTGGGATTA CAGGCACCAA CCACCATGCC 60 TGGCTAATTT TTGTATTTTT AGTAGAGATG AGGTTTCACT ATGTTGGCCA GGCTGGTCTC 120 AAACTTCTGA CCTCAAGTGA TCTGCCCACC TTGGCCTCCC AAAGTGCTGG GATTACAGGC 180 GTGAGCAATT GTACCTGGCC CCTCTAGGAG TACTTTTAAT TCTGCGGTTG GAGCAATAAG 240 AGAGAAGGAG AAACTCCAAA ACTGTCCTAA TTGATTCTGA GCCTCCCCTC TCTAGAAACT 300 GGCCTGGACT AAGAATAGAC CGCCCTGCCA CAAGCATCCA CCCTAAGTGT TTCTGGTTTA 360 CATTGCCCTC TTAGGGCCTC TGAGACTCTC CTCAGGTTCG GTGTTTTCAT AGCAGAGTGC 420 TGTCTAGCCT GTTCACATGT CCGTCCTGCA TTCTGAAGCC CCACTCTCTG AGCCAGGGGA 480 GATCAGGGAC ATTCTTGAGC AGAGCCAGTG CAGGGAGTGC ACAGTCCTGG AGCAGGTAAA 540 GACCTGGAGC AGCAAGTGAA AGACCCAGAG CAGAGGATGA CATGGAGTGA CAGCAAGAGG 600 TTAGAGGGAA GTCTCAATCT CACTTGGCAT CATCTAGCAG AAAGACCAAT GAATTAATTT 660 GAGGTTAGTT CGTGTGGGTC CTGAGGCCTG CAGACAGTGT GGGGTAACAA TACTAATGAT 720 GAGAGTGATG AGTGTCTCCC GTGGCCGTGT CCTCTCTGAA TCTCTGAGCA TTTTATCTTT 780 CATCTCTGTG GGAGTTGCGG CTTAGTAATA ATAATTAGAG TACCCTGAGC ATCGGTGCTT 840 TGTAGAACAC AGCATTAAGC CCTGTTTCTG CCTCCTTGGA GTGTAGTCTG TATGAACTGG 900 CAGACATTTG GGAGGTGGAG CCCTCTGACA GAGGGGAAGA ACATGATAGA ATGCAAAGGT 960 CAGGGATATT CTGAGTCACC TAATTGATAC CTAACATTCT TTTGGCTCTT GGTAGGTCAG 1020 AGTGGCCTTT CCTTCATGCC TGCCAAAGCA CAAAGATCAG TGGCCTCACC CAAGTCTCAC 1080 AGACCCAAGA GTCTAGTCTG GGGATCCCAG GCTCTAGCTT ATACATGGTA CCTTCCTGGT 1140 TTTGGGGAAT GCTTGTTCCT CTGTGGCCAT GAGTTATGCT TTAACGAGTT GGTGTTCTTT 1200 CCTGTGGTAC CAGCAGACTG AGCCCTGCCG AAAATAGGTG ATGCACGCTG GGTTTTTCCC 1260 GTGTGATCAA GAAGCCCGGT GGGCAGAACA GAAGAAGCTG CAGAAGTCAT AGCTCCATTC 1320 TCCTGAAAAC ATGGGTGTCT GGAAAGTAGC CAGTGCCTCA GGATGGTCCC AAGTACCTTC 1380 AGCACCTTCT TCCCAAACAC ACTCTGTCTG TAACATGTCA CTTCTCTCTT CCTCTAACAG 1440
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