Tag | Content |
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EnhancerAtlas ID | HS118-16935 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr7:927160-929400 |
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) |
HSF1 | MA0486.2 | chr7:927452-927465 | TTCTGGAACATTC | + | 6.67 | Myod1 | MA0499.1 | chr7:927934-927947 | GGGAGCAGCTGCA | - | 6 | Zfx | MA0146.2 | chr7:928913-928927 | GGAGCCCAGGCCTG | + | 6.22 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_01342 | chr7:927412-929403 | Adrenal_Gland | SE_31777 | chr7:928564-929435 | Gastric | SE_41630 | chr7:921336-929364 | LNCaP |
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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 |
GH07I000887 | chr7 | 927413 | 929435 |
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Enhancer Sequence | GCCTGGGGCC AGGGCAGGCG TGGGCACCTC TCTGCTCTCG GCGTTGATTT GCACTGTGCG 60 TTCCAATACA TCAGGGTCAC CCACCAGGGC AGAGATGGGG TTTCACCCTG TGGTCACGCG 120 GGCCGGTCCA TGGAGACCCA TGCGCCATGC TAAGCCCGGG ATCAGAGCCA CTGCACCCGA 180 GAAGCTGCGA GAAGGGGGGC AGGCGGCCGC CTCTCCAGGC CTTCCCGTGG GACGTTCTGA 240 CCCTCAGGGA GGCAGCCGTG CCTTCACGGG GCCTATGCGT GCTGCTGCTC CTTTCTGGAA 300 CATTCTTTCC AGCGCTGGGA TGGTGCTGTG CCCTGTTTTT CTCCTTTACG CTGACCTCAT 360 CTTCTGATGA AGCCTTTGCG GGGATTAATC ACCCTGTGGT GGGGTCTGGC TGTCTGCGTG 420 GTGTGGTTGG TGTTTTTAGT TCCAGGTCTG CAGCTCTGAG GCGGGAGTGG TGCTGGGTAG 480 ATATTCATTG AGTGACTTGA ACGAGGTGCT AATGGGGGTT TAGAAGCGTC CTCCCCAGGG 540 CATTCCCTGG GATGGCAAGT GGCACCAGCG CTGTGAGATG GTTTCCTTCC TGCCGTCAGG 600 CGTCAGGAGG CCTGCTCGGG TCTGCATGTG CCTGGGCTTG GCAGGTGGGG AGGCGGCACC 660 CAGGGCAGCC CCCGCATTGG AAGCTCTAGG AACTTGGATC TAGGCTGAAG GCCTTTGCTC 720 TAGAGTTCCG GATTGCTGAG CTTGGAACAG CTCCTCCTAG ACACAGTGTG GCGCGGGAGC 780 AGCTGCATGA GGGCCCACGT ACTCTGCACA CATCAGCAGC CCATCCGACC TTGTCCCTGG 840 TCATGCGAAA CGCATGCCCA TCCGACCTCC GACCTTGTTC CTGGTCATGC AGGTTCCGCC 900 TGGGCTGTGA CAGGAGGCTC GGCGCCCTCA GGCACCTGGC AGGCTTTCCC GACCTTCTCC 960 CTGAGCGACA GGAATGGGAA GTGAGCAAAT CCAAGTAGAA TTAGGAGGCT CTCCTCAGAG 1020 GAGCCTGGCG GAACCCGGTC CTGGCTGTGT GCCGAGTGGC GGGGCACCCA CAGGGAGATG 1080 AGCCAGTGCC TATCTCTTGC CTCAGTCTCC CCGTGGTCGC CTCCTTCCTC AGAAGGGGCT 1140 GGCCCAGGCT GGTGCCTCCG TGGCCCCTGG AGCATACCTG CTGCCGCCTT CCCTGGCCTC 1200 TGGCGACAGC AGGCCTTCCG TACTCCACCT GTCCCCCAGC CAGCATGGCT CCACACAGAA 1260 CACGGCCGCA GACAACCCTC CTGTGTCCTG CATAGCGAAC TGCCACTCTG CGTGGGCCCC 1320 ACTGCCAGGT TAGGGAGGCA GGAGCTGCCC CCACCCCCTG CCCGGGAGCT GTCGTCTGTC 1380 TTTCGGATGA GTCAGGAACA AATGCGTCAA CACTGGGTGG CCGCCCTCGC CACTCCTGCG 1440 CACGGGCCCT GTGGGGAGAG CCAGGCAGTG GGTGGCGTGG GACAGGTGAT GCCCATGCCC 1500 AGTACTCAGG AGACCTGCAT GGCAGCTCCT AAGATGGGTA CAAGCGATCA TAAGGAGGGA 1560 TGTACGTGTC TCATCTCCCC ACCCACCACG GGATCAGGTT GAGGCCGTCC AGGGAGTGCA 1620 TGGGAGGGCT GCGCTCGGCG CATCTGCAGA GATCCCCTGA AGAGGGGCCC TGGCTGCCTC 1680 CCACTGGGGT AGGTGCGGGC CCAGGTCCCC GACACCGTGA CGGTGCTGTG GGACTTTGAT 1740 GGACCTCACC CGGGGAGCCC AGGCCTGCTC CACGGCAAGG TGGCCACGCA CTGCCTCTGC 1800 AGTCCTGAGC ACAGGCTCCA TACGGGACCT GAGGCCTGGG CTCCATGACA CTTGGGCTAT 1860 GTGCTTCCCT GGTGCTTCCC TCCTGGGGAT GAAATCACAC CCATAGGTAA AGGTTTGGGA 1920 GTGGAGGGAG ACAGCAGGAG ACAAAGCAAG GGGACGAGGA CTCTGGCAGC CACAAAGGCA 1980 GCGGGAGGGC CCTGGAGGCT CCTGTTGGGC AGCGCAGTCA GGAAAGGGCC CACTAGGTGG 2040 GAGAGGCAGG CGCCTGGTGA GTGCTGAGAT CTGCACCACG AGAAGGGCTG GGCTCCCAAG 2100 GCATGCATGG GGCCTGGGAG TGGAGGGAGT GTGAGCGGGT GTTAGGACGG GGTCTGGGGC 2160 GAGCGGGTGT TAGGACGGGC CTGGGAGCGG AGGGAGTGCG AGCGGGTGTT AGGACGGGGT 2220 CTGGGAGTGG AGGGAGCGCG 2240
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