Tag | Content |
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EnhancerAtlas ID | HS095-28595 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr7:127803170-127805830 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr7:127804618-127804631 | TGCAGCTGTCCCT | + | 7.82 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH07I128163 | chr7 | 127803702 | 127805450 |
| Enhancer Sequence | GGGGGGCTGC AGCACCTTCG CTGCCAGACA AGAGAGGCAA AGAAGGGGTC AGATGGAGGG 60 TCTGTTGGAA AGGAGAGAGT CTGTGGCCAC CAGAGGCCCA GCCAGCCAGA AGCCAAATCC 120 CAAGAGGGTA TCTCACTCGG CCATCTGCCC ACCTGTAGCC CCTGGATTTG AGGGCCATTG 180 ATTCCTTGGC TGGGCCAATT TCCACTGCAG TCGAGGTCAT TGCCAGGTCT CCACGTCTGT 240 GCTGATAACT CTGCTTGATG ATCCCTTTCC TCCAGTGTAT GAAGGAGGTG GTGAAAGGAA 300 TTGCAGGGAA GGAGCATCAC TTATCTTGAG TTATACCAGG ACCTAATGGC AGTCCTGGAA 360 TCAGAAGCCA GCTCTCTTAA TTCCTGACCA GGCTCTTTCT TCTTGACTCT GTTGCCAAAG 420 TTAGTCACTT TGCCATTGTG GGGCTCAGAA CAGGGCCTCT GGTTGGGGAC TGGGGGGCTC 480 TCCTCCTGGC CCATGTTCAA CAGGAGGTCC CGGGTCTTCC CTGGCTGAGC CTATTCTTGC 540 AAACTATGTG GGGGCTGATG TAGGACATAG AGTGGCCTCT GGGGAGACAG CCTTGTGGAT 600 CCTCACTAGG TCATTGGCCC TTCTGGCCCC ATTGCCATCA GCGTCATATA GTGAGATCAG 660 CTGCCTCCAA GCCCCATGGG AGGCCTGGTG TGAAGAGCTC AGCTCAGCAA TGAAACCTAT 720 GGCCCATGTG ATCAACAACA TCCTGATCTC AGCAGACTGC TGATAGAAGG AGAGGTTAAG 780 ACCTATTCCA GAGCATGATT GGATTGGACA AGACAGCCAA GGTGCTCAAC ACATCAAAGA 840 AGTCTTTCCA CAAATGTGGC CATTCCTGCA GTGCTGCCAT GGGGGAGCCA CGACAACTTC 900 AGTTCAGGCA ACAACCCTCA CCCCTCAATT GTACTCCAGC CCAGGTGACT GGGCCTGTGG 960 GGAATGTCTA ACCCAAGGGC TGTGATCTCT GGACACCCCA GGAGCCTAGA AGTGGCCTGA 1020 ATCAGAGGCT CTCATTAACC TGGTGCCGAC CTGAGTCATT CTGATTCTCT CCTTCATAGT 1080 AATTTGAACT GGAGATGTGG TGAGAAAGCC AGAAGGAGGC AGGGACAAAT GAGTCATGAG 1140 CAACCTTCAG CGCAGCACTC CAACCTGGCA TCTTGCAGCT CCTGCTGCCT CAGAGCTACA 1200 AGATAGCCCA GGGAGTCAAT AGAGCCCCAG TGCCAAACAG CATTCCAGGT TCCCAGCCCC 1260 CTTCCCCTGG CCCCACCCCG CTGCATTCCA ACGATAGCTA AGTCTGAACA TACCTGGACT 1320 CCTAATTCCC TCCTACCCTT GTGCCTCCTC ACAATGAGCC TGGTTACCTG AAGCAGCCTG 1380 TTACCAAAGG CCCCCTCAGT GGCAGCACAG ACACTACTGG GGAAGAGCAT CTCAGAGGCA 1440 AAGTGGGGTG CAGCTGTCCC TCCCACACAG AGAACTCCTC CACTCCCACC TTGGAGGATA 1500 GGGAGTGTTA CATGAGGAGA CCCGGCAGGC CCCTGGGACT CACAGGCTGC CATCAATGTG 1560 CTGACAGGCC TGGGATGCAA GGCTGAACAA CCTGGGGCAA CAGTGTGTCC AAGATAGGGC 1620 TGGGCCACAG AGAACCAGTC ACTAGCCTGC ATGTGTGTGC TGGGCAGGCA GCTGCCACAT 1680 CCTTGCTGGC TGAGTCAGAC CCCTTGGTCA CTGAGTCTCC AGTTTATTGT TATTCACTGA 1740 ATAACAGAAG TTTCTGTGGG CCCAGATGAG ACTGGGGTCT GTCTGTCTTG TGATTGTAAG 1800 GCACTGGCTT TCCTGCCAAA CAGCTCATTG CGCAGATCCA GGGCCTCTCT CCTTGGACCT 1860 GGGTGGACTC CAGGATCTCC TGCTGAAATA GCCAGGCCTC TCCTAGCCCA GGTCTTCAGA 1920 GATATCAACA TCAGCACCAC TCTGCATCTC AGGACAGGCC CTCGGCTGAG AGACAGTAAG 1980 CAGATTGCAG AGCTTCCTAG GCACCTACTG TGTGCCTGAG TGGCACAGCT GGGCCACATG 2040 GAGCACATGG AGATGGGTGA GACCAGCTTC CAGCTCTGAG AAGTTACAAC CCAGCAGGGA 2100 GATGTGCAGC TTAGAGAACT AATCATCCCA CATTGACACT GCAATGTGAT CAAAGCCTTG 2160 AGAGCCATTC CCCATGATCC AGGGACTAAC GGTAGGTGAG CTCATAGCTC TGGGGATCAG 2220 AGAGGCCTGC ACGGAGGAAT CAGCATTAGA CCTGGGTTTT GGCGGCTGCA TGGACTTCGA 2280 CATGGAGAGG TAGATGGGAG CAATGGACTG AGGCAGTAGG TTCCCAAAAA AGGGACTTTC 2340 AATCTTTGCT GACACAACAT TAATGTCAGT TGTGCCCAGG ACTGTGCCAG AAGCAGCTGG 2400 GGGAACAGAG GTGAGTGCCA TGTGGTCCCT GCCATGAGAG AGGGCCAAAC AGGCAGATTT 2460 TGGCTGCAGC TCAGTGGGAC AGGAGCTGCA GGTGAGGGAA GGGCAGCAGC GGTGGAGCCC 2520 AGCAAAGCAG CCTTGGTGCA TGTCTTGCTG GGAAACAAGC ACAGAGAGAG GGAGGTGGAG 2580 CCATAACCTG ACCCTCCCCA TCTCCACTTG ATTGAACCTG AATCTGAAGG CATTGGAGAG 2640 CTGCTTTCGG AAGTCTGGAG 2660
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