Tag | Content |
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EnhancerAtlas ID | HS089-03675 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr12:121351890-121353270 |
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) |
HES2 | MA0616.2 | chr12:121352016-121352026 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr12:121352016-121352026 | GGCACGTGCC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr12:121351934-121351949 | GAGGTCAGGAGTTCA | + | 6.22 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_27043 | chr12:121352024-121353293 | Esophagus |
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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 |
GH12I120914 | chr12 | 121352192 | 121353043 |
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Enhancer Sequence | ACCTGTAATC CCAGCACTTT GGGAGGCCCA GGCGGGTGGA TCACGAGGTC AGGAGTTCAA 60 GACCAGCCTG ACCAACATGG TGAAACCCCA TCTCTACTAA TAATAGAAAA ATTAGCTGGG 120 CATGGTGGCA CGTGCCTGTA ATCCTAGCTA CTCAGGAGGC TGAGGCAGGA GAATTGCTTG 180 AACCGGGACC CGGGAGGTGG AGGTAGCAGT GAGCCAAGAT CGCACCACTG CACTCCAGCC 240 TGGGTCCAGC CTGGGCTACA GAGCAAGACT CTGTCTCAAA AAAAAAAAAA AAAAAAAAAA 300 AAGGGACGCA ACCACGGCGG AAGAACAACT GCCAGTCTAA CTGTGCGTGA AGGCTGGCAG 360 TGATGGGGCC GAGACTGGGA ACCGCCCCTT CTCCCTGAGA CTGTTCATAG TGCTGTGGGT 420 CACAGGAGTC ACCTTCAACG TTACCACCAT TGACACCAAG AGACAGACTG AGAGAGTGCA 480 GAAGCTGTGC CCAGGAGGGC AGCTCCCATT CCTGCTGCAT GGCACTGAAG TGCACACAGA 540 CACCAACAAG ATGGTGGAAT TTCTGGAGGC AGTACTGTGC CCTCCGAGAT ACCCCAAGCT 600 GGCAGCTCTG AACCCTGAGT CCAACACAGC TGGGCTGGAC ATATTTGCCA AATTTTCTGC 660 CTACATCAAG AATTCAAACC CAGCACTCAA TGATAATCTG CAGAAGGGAC TCCTGGAAGC 720 CCTGAAGGTT TTAGACAATT ACTTAACATC CCCCCTCCCA AAAGAAGTAG ATGAAACCAG 780 TGCTGAAGAT GAGGGCATCT CGCAGAGGAA GTTTCTGAAT GGCAATGAGC TCACCCTGGC 840 TGACTGCAAC CTGTTGCCAA AGCTACACAT AGTACAGGTG GTGTGTAAGA AGTACCGGGG 900 ATTTAACATC CCTGAGGCCT TCCCGGGAAC GCGTCAGCAC TTGAGCAATG CTTATGCATG 960 GGAAGAACCC GTCTCCACCT GCCCAGATGA TGAAGAGATC CAGCTCGCCT ATGAGCAAGG 1020 GGCCAATGCC CTCAAATAAG CCCCTCCTGG GACTCCCTCA ACCCCCTCCA TTTTCTCCAC 1080 AAAAGCCCTG GTGGTTTCCA TATTGCAACC CAATGGACAC ACTCCAAAAT GGCCAGTGGA 1140 CAGGGAATCC TGGAAGACTT GTTCTGGGAT GGTGTGGGGA AGAGGGGATG AGGGAAATAA 1200 ATGGGGGGCT GGGTGAGATT TTTATTGTGG GGTGGGATGG GCAGGACAAC ATATTTCAGT 1260 AATAAAATAG AGAAAAAAAT GAAAAAATAA ATAAACAGCC GCATCTGTTA AAGAAATAAA 1320 GAAAAAATGT AAATACAATT TAAAAATATT TACTCACCTG TTTACCATCT CAAGAATTTT 1380
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