Tag | Content |
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EnhancerAtlas ID | HS105-20793 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr12:120538040-120540200 |
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 | chr12:120539302-120539323 | ATGCAGTTTCAGTTTCTCTCT | + | 7.22 | IRF9 | MA0653.1 | chr12:120539306-120539321 | AGTTTCAGTTTCTCT | - | 6.28 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_27057 | chr12:120537449-120541185 | Esophagus | SE_31982 | chr12:120538202-120540645 | Gastric | SE_41982 | chr12:120537882-120541422 | LNCaP | SE_68937 | chr12:120538843-120541016 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 120538251 | 120539859 | chr12 | 120539953 | 120540181 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I120099 | chr12 | 120536948 | 120540903 |
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Enhancer Sequence | CCCATCAGCT CTCTGGCCAA TGCTTCACAT CTGAGGCCCG ATCTAAGGAC AAAGACCAAC 60 CCTGGCTCCA TCTCTGAAAG GCTGGCCCTT GGGAAGGTGC CTGCATTCAC CCTGCCACAC 120 CTTGCAGCTT CAACAGTTAT AGCACACAGG TGGCTAGTCC TTAACTGGGG TGGTCATGAG 180 GAAGAAAGGA GCTAAGCATT ACCCCAAGGC GGGGGAGCAG TAAACAGTCA GTATGCGTTC 240 TTCAGCATCA TCAATGTGCC TTCAAGGACA ATCTGTGGTC CCAGACAGAG GTGGTGGAAG 300 GAAACCAACA GGCAGCTTAG GGGCAGCCCT GAGCATCTTC CCTGATGCTG CAGAGCCAGA 360 GCTCCTGCCC AGCCCTGGGA CAAAGCCCAA CCTGCCCCTG CCACCGCCCC TGCCCCATCC 420 TTGCTCCATC CTCAACACGA CCGCTGGGAT CTCTTCCCAG GGCTTCATTC TGCCCACAGC 480 TTTGCTTCCA GGGCAGCGTC GCTCCTTGGC TTCGGGGTAG CTGTGACGAT CAAGCTCTCT 540 TGGCACTGGG CCCAAGAACT AGCTCTGGCC TTGGCAGCTG CTGCTGAGAG CGCCGGGTCA 600 GCACATGGCA TGGTGTGTCA GACGCCTTCC AGAGCGAGGG CGCGCCGGAG CCACAGGAAC 660 AGGCGACTGT CCCCTGCCAG CAGAGGAAGC CCAAGGAGCG GATGGCTCTG CAGACTCTCC 720 TTTGCTGAAG ATGATCAGAG ATGCCAAGAA ACGCCTGCAG CCATGGCCCC GGCGCACAGC 780 CCCCGCGGCT CCCTGGGCGC CTCTGCCTCA TCCGGGGCCC AGGAAAGGGG CTTTATCTGA 840 GAGCAGAGAA TTTGTCTGGG GATGAAGTCA GGGGCTCAGA GCTCTGGCTA GGAGGAACCG 900 GAGCACCGAC GTTTCCCATG GCCACCAGGA ATCACCTTCA CTCACAGGGA CTCTGCTCTA 960 GGCCAGGCAC AGAGCTGGGG GCTTGGTATC CATTACCTTA TTAATGTCTG CAGCCACCTG 1020 ATCCAGCAGA CCTCAGGATG GCCATGTGAC CAGCAAGGAC GTGAGGCTGA GTGCAGCGGC 1080 CAGCTGGAAG TCCTGGCGCC CAGGGCTGAC TCCCAGGCCC AACGCCAGGG CCTTGCCTTC 1140 CTTGTCACTT CTCCCCTCAC CTCCATCCCA CCCGCACCTC TCAGGGCCGG CAAACCTCAG 1200 CTTCTGAGAG CAAGAACCCG AGAAGGGGTG ACCACAAGGC TTTTTCTCGC CAGGCTAACA 1260 GGATGCAGTT TCAGTTTCTC TCTGAACGCC CTGCATCGGA AAAAAGTCAC GCTACTGCAT 1320 CCTGACTGCC CTATTCCTGA AAACTCCTCA CCTCCCCAAA ACTCCTTCCT TCTTTGCCAG 1380 TGACCATCAA AGGGCGTCGA GACTTCCAGT GGCCCCTCAG GGCGCCCTGC TGGGCCTCCT 1440 GCCTCATGAG GGCCAGAGCG GGACTCTAAG ATGGAGCCAC CTGTCTGCTT CCCCAGACAC 1500 GTGGGACGGC AGCAGGGGCC CAGCCGCTGC CCACAGGCCG CCCCTTCCCA AGCCCCTGGG 1560 GAAAAACCCA TGTTGCTCCC AGGAAGCTGA GTGACTCCTC CCCGCCTCCC CACGGAATGG 1620 AGGAACCAGT TCACCTTCTT CCCGCTCTGC CCAGCCCAGA AAGCAGCTGA CTGCATGATG 1680 GCAGGGAGGG GCTGTGGCTC CTCCTGCTGA AAGAGCCTCG GACCCCCCAG GCCCCACTGC 1740 CCTGCCCAGG AGTTCATTCC TCATGGCCAC GGGCCTCTGA ACCTCTGCCA CCCTGAACCT 1800 CCGCCTGGTT TTAAGGCACA GGACGGGGCA GGAAGGCAGG GGCGCCACCT GCCCAGTCGA 1860 TGCAGGGCCT CGGCAGACTC AGGGCCAACC CTGAGTGCCC CCAACCTCTG CCCCACTGAG 1920 TTAGGAGGCT TCATCCTCCC TGGGCCTGTT TTCCTGTCCA TAAAATGGAG ATAGTCACAG 1980 GTCTCTCTAC CGGGATTAAC CAAAATAAAG CAGCTGAAAT CCTAGCGACA GGACCAACCC 2040 AGAGCAAGGA TTCATGAGGT CAGCGCCCAG ACCAGCCAAC GGCATGAGGG CTTGCCTCGC 2100 CTGGGCCTGC AGCCCCAGGC TGCCCAAAGC ACTGATGCCA GCCCTGCCCC AGTGTCCTCC 2160
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