Tag | Content |
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EnhancerAtlas ID | HS120-06246 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr9:98256160-98257210 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr9:98257056-98257077 | AAATAGAAACAGAAAGAAACC | - | 6.49 | NRF1 | MA0506.1 | chr9:98256433-98256444 | CGCGCATGCGC | - | 6.02 | NRF1 | MA0506.1 | chr9:98256404-98256415 | TGCGCAGGCGC | - | 6.62 | ZEB1 | MA0103.3 | chr9:98256342-98256353 | CCCACCTGCCC | + | 6.14 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_03132 | chr9:98256333-98257702 | Bladder | SE_07266 | chr9:98255688-98257908 | Brain_Hippocampus_Middle_150 | SE_31685 | chr9:98256017-98257680 | Gastric | SE_50225 | chr9:98256044-98258846 | Sigmoid_Colon | SE_59533 | chr9:98255300-98274932 | Ly3 | SE_60316 | chr9:98255143-98274439 | Ly4 | SE_60774 | chr9:98254465-98274452 | DHL6 | SE_63271 | chr9:98255915-98274757 | GLC16 | SE_63468 | chr9:98255894-98279218 | NCI-H69 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I095493 | chr9 | 98256086 | 98259405 |
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Enhancer Sequence | ATCTCTTTTA TTCAGGAGGA GCCAACCGCT GTCCAAGTTT CTGGGCCGTT TTTTTCCTTA 60 TGAGATTGTG CCCCTGCGTG TTGCCATGGG AAAAACGCTA CAATCAGCCC AAAGAGAATG 120 TGCCTTCATG AAGTGAGCCC AGTGAGAGGT CAACCACCAA AGCATAACGA GAAAAGGACA 180 CCCCCACCTG CCCACGGAAC CGCACGGGAC CGCACGGGGC ATGTGGCAGG CTGGGCGCAG 240 GTAGTGCGCA GGCGCTCGCG CGGGGTTCTG CAACGCGCAT GCGCCGGAAG CAAGCTTCCC 300 CGCCCCCACC AGCTGCTGGC AGTGCCATCT GTTATCAGCC TTGCCCAGGC TGCTCCCTCT 360 GAATGGCTTT CCCTGACGCA GACCTGCTCG CCCTGTCAGA TGCAATCAGG TCAGCCCGGC 420 ACTCTGCCCA CGCTGGACCT GCTGCCTGTC GCAGCTCCCA CCAGCTCCCA AGGAGCCACG 480 AGTTCCCGAG ACGACGCTGC ATCTGCCAGG AGGCCCCTTC TTCATTGGTT ACTTGCCACA 540 CTGGCAAATG AGGGCTGTGC ACCGCGCCAC CTGAGACAGG CCCAAGAACG TTGCTGACTT 600 CCTGCAGAGC ACAGGCGGAA ATGTCTTCCA TCCGGAACAG CGTACTTTCC AAGCTGGGAA 660 CTGTCCCAGG TTCTACCACA ACCTCAGGTG CAACCAGGCC GCTCAAGCGC AACAGGCAGG 720 CAGATGCACA CCCAGGTCCC GTCGCTCTGC AGGAAGTGGG CGGGCCCAGA GGTGTGATGA 780 CGAGCGCGCG CTGGCTCAGA GGCCACACTC CAGCAGCAGC AGGCAGCAGA ACCCAGGAAC 840 CAACACAGCG TGTTTTCATC AAGCTTAGTT GAAACCTCCT GAAGTCTTCA TTAAAAAAAT 900 AGAAACAGAA AGAAACCCAA CAACAACAAC AAAACCCAAG TGCTTCCACG GCAGGCTCTC 960 CATCACAGCA CTCAAGGCAT TGCATAACAT TAACCCCAGT TTCCTTCTCT CAGCTTCTGT 1020 GGGGCTGACA TCACCTCTCA GCTCTGAACA 1050
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