Tag | Content |
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EnhancerAtlas ID | HS034-30666 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr9:98256310-98257530 |
SNPs | Number: 1 | 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 | CAACCACCAA AGCATAACGA GAAAAGGACA CCCCCACCTG CCCACGGAAC CGCACGGGAC 60 CGCACGGGGC ATGTGGCAGG CTGGGCGCAG GTAGTGCGCA GGCGCTCGCG CGGGGTTCTG 120 CAACGCGCAT GCGCCGGAAG CAAGCTTCCC CGCCCCCACC AGCTGCTGGC AGTGCCATCT 180 GTTATCAGCC TTGCCCAGGC TGCTCCCTCT GAATGGCTTT CCCTGACGCA GACCTGCTCG 240 CCCTGTCAGA TGCAATCAGG TCAGCCCGGC ACTCTGCCCA CGCTGGACCT GCTGCCTGTC 300 GCAGCTCCCA CCAGCTCCCA AGGAGCCACG AGTTCCCGAG ACGACGCTGC ATCTGCCAGG 360 AGGCCCCTTC TTCATTGGTT ACTTGCCACA CTGGCAAATG AGGGCTGTGC ACCGCGCCAC 420 CTGAGACAGG CCCAAGAACG TTGCTGACTT CCTGCAGAGC ACAGGCGGAA ATGTCTTCCA 480 TCCGGAACAG CGTACTTTCC AAGCTGGGAA CTGTCCCAGG TTCTACCACA ACCTCAGGTG 540 CAACCAGGCC GCTCAAGCGC AACAGGCAGG CAGATGCACA CCCAGGTCCC GTCGCTCTGC 600 AGGAAGTGGG CGGGCCCAGA GGTGTGATGA CGAGCGCGCG CTGGCTCAGA GGCCACACTC 660 CAGCAGCAGC AGGCAGCAGA ACCCAGGAAC CAACACAGCG TGTTTTCATC AAGCTTAGTT 720 GAAACCTCCT GAAGTCTTCA TTAAAAAAAT AGAAACAGAA AGAAACCCAA CAACAACAAC 780 AAAACCCAAG TGCTTCCACG GCAGGCTCTC CATCACAGCA CTCAAGGCAT TGCATAACAT 840 TAACCCCAGT TTCCTTCTCT CAGCTTCTGT GGGGCTGACA TCACCTCTCA GCTCTGAACA 900 GTCTTCTTGC CATTATCCAG CCTGGGCCTC TCTTCATTGG CCTCCCACTT GAGCCGACAT 960 GGGGGAGAAG ACAATGCGAG TCTCCACCTT CGCACGCAGG CTCCCTGGCC TCCGGTGAAT 1020 ACCACGCTGG CCTCATTTAT CTCCTGCACT GTTCCTTCCC TCTGCATCTG TGCAGGGAGA 1080 CTCACGTCAC TGGGGGCCAC TTTCATGATT TTGTTGCCAT CAGGATTAGC TGGATTAGGG 1140 GCCAGTACAT AAGGACCCCC TGGTGCCGTG AGGAAGTTTC ATCACCGGGT CAGCATGGTG 1200 TGAACTATAT TCTGTCAACA 1220
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