Tag | Content |
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EnhancerAtlas ID | HS139-15179 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr13:52657490-52660410 |
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) |
SP2 | MA0516.2 | chr13:52658198-52658215 | TTAGGCCCCACCCACTT | + | 6 |
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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 |
GH13I052085 | chr13 | 52659245 | 52660119 |
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Enhancer Sequence | TTAACACAAA TTATACACAG TCAACAAGAT TGGTTCTGAG TGAGCTCTGA AGGCTACTTG 60 GCTGATGCGC GATCAATGAT GAAATGGCTG GACAGAACCC TTTTTATAGC TCCTTTTCCC 120 CGCCACAGCT TCAGTATTTC CCAAATCCTT CCTCCATAGC CTCTGTAGAA ATGTCTGATA 180 TCCACCATTT TTTTTTTTTT GAGATGGAGT CTCACTCTGT CACCCAGGCT GGAGTGCAGT 240 GGTGCGATCT TGGCTCACTG CAAGCTCTGC CTCCTGAGTT CATGCCATTC TCCTGCCTTA 300 GCCTCCCAAG TAGCTGGGAC TATAGGCACG CACCACCACG CCTGGCTAAT TTTTTGTCTT 360 TTTAGTAGAG ACAGGGTTTC ACTGTGTTAG CCAGGATGAT CTCGATCTCC CGACCTCGTG 420 ATCCGCCCAC CTCAGCCTCC CAAAGTGCTG GGATTACAGG CGTGAGCTAC CGCGCCTGAC 480 CAATGTCTGC TATCCATTTT TGCAGGGCTC AGGCTGCCCA TCCCAGATCA GCCTTAGACA 540 TAAGGCTGAT GATGGCTCCA GGCTGCCCAT GAGCCAGGCC TCTGCTCCAG AGAGAACAAC 600 CTCCAGGCTG CCCCTCCCAG CACACACAGT CCTCTGTCCC AACCTTTGCA TGGTTCTTTC 660 AGAATGCCCA CTCTCCTCCT TTAACTCTGC CTCTCCAAAT TCCACTCTTT AGGCCCCACC 720 CACTTCTTCC ATAAATACCC GCTACCTGCT CATTCTGCTC ATCTTGGCTC CTGTGCACCT 780 ACAGGGCTTA CTCTATGATT GTTTTATACA TGTGTCTCGT CATTCCAACC ATTTATAAGT 840 AGAACTGCAT ATGCCAGAAA GAATAGTGGT TATAATTGTA TTTTTTTATT TTTTGGGACA 900 GGGCCTCCCT CTGTTGCCCA GGCTGGAGTG CAGTGGAAAA ATCACAGTTC ACAGCAGCTT 960 CAACCTCAGC CTCCCAACTC AGCCTCCTGA GTAGCTGGGA CTACAAGCAT TTGCCACCAT 1020 GACCCACTAA TTTTTTAAAT TTTTTGTACA TATGGAGTCT CATTATGTTG CCCAGGCCGG 1080 TCTCAAACTC CTGGGCTCAA GCGATCCTTC TGCCTTGGCC TCCCAAAATG CTAGGATTAC 1140 AGGCATGAAC ATGAGTAGGG GTTTTAGAGT CAGATTTTCA TTTTATTTTA CTTTATTTTT 1200 TTGAGACCGA GTCTTGCTCT GTATCCCAGG CTGGGGTACA GTGGCACAAT CATGGCTCAC 1260 TGCAGCCTTT AGCTCCTAGC TCAAGCAATC CTTCTGCTTT AGCCTCCCAA GTAGCTAGGA 1320 CTACAGGTGC AAACCACCAT GTCCGGCTAA TTTAAAGAGA GAGAGAGAGA GAGAGAGAGT 1380 GAGAGAGAGA GAGAGAGAGA GAGAGAGAGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT 1440 GTGTGTGTGT GTGTGTGTGT GTTTAGAGCT AGGGTTTCCC TATGTTGCCC AGGCTGGTCT 1500 CAAACTCCTA GGCTCAAGCA ATCCTCCCAC CTCAGCCTTT CAAATTGCTG GGATTACAGG 1560 CATGAGCTAC CGTGCCCAGC CTAGAGTCAG ATATTTAAAT ATTTCGTCTG CCTTGTAATA 1620 GCTACGTGAC TTTGGATGAG CTACTTAACT TCTCTGTACA GGGGTAAATA AAAGAAAGTA 1680 TGAACGTGAT ATGGTTTGGC TCTGTATCCC CACCCAAATC TCACCTTGAA TTGTAATAAT 1740 CCTCATTTGT CAAGGGTGGG GCCAGGTGGA GATAACTGAA TCATCGGGGT GGTTTCTCCC 1800 ATACTATTTT AATGGTAGTG AGTAAGTCTC ACAAGATCTG ATGGTTTTGT AAATAGGAGT 1860 TCCCCTACAC AAGCTCTCTT GCCTGCCTTC ATGTAAGGCA TGACTTTGCT CCTCCTTTGC 1920 CTTCTGCCAT GATTGTGAGG CCTCCCCAGC CATGTGAAAC TGTGCGTCTA TTACACCTCT 1980 TTTTCTTTAT AAATTACCCA GTCTTGGGTA TGTCTTTATT AGCAGTATGA GAGCAGACTA 2040 ATACAGTATG TGAAAGCTCT AGTTCATGGC CTGGCAAACA CAACTGAATT GCACCATACA 2100 TTCATTTGAC TTATATGAAT TTATCTGTAT GCACTGCGGT GGGAGAAAGA GAGAGAGAGA 2160 TCAATTTCAG CAGCATGGTA GCTCTACTCA ATGAGTGTGT GGCCAAGTGC ATGTGGGATG 2220 GGAGACAGCT GTCTCAGTGC CTGCAAGCTT CTCCTAGGAG AGCATTCCAG GGCACTGAGT 2280 GTGTTCCTAG TGTTTCAATA GCCATGTGTC TTTCTTACAA CATGGTTTCC AAACACAGGC 2340 TGGCTATTTC ATGTGAAGCT CTTCTGAAGA AGCAGTGATC TGTGCCAACT CTAGAGACCT 2400 TCTTGGGAGA TGGAAGGATG AATTTCCAAT GTGGCGCCTT TAAGAGATTT TTAAGAATCA 2460 GTTCAACTGC ACTCAGATTT TGCCTTAAAT AGCCTTTAGA ACCTTACCCT GCAGAGAGTT 2520 GAAAAAATGC TAGTGTGTTG GGTTTGTTTT TTTCCCACCT TCTGGGCATG AACTTACACT 2580 CATTTTGGAC TTTCTGCATC TAATCCAGCT CTGGTCTAAA GTTGCCACTC AATAAATATG 2640 TATTGAGTGA TTCATGAAGG AAACAATCAA TAAGTACTTT TAATAATAGC CATTCCTGAG 2700 AATCTCAGAT ATCCTTATTA TCTTGTGTAG TCTCTCATAA ACCATAATAA ACTGAAGCTC 2760 CAATGAGGTC TGACAGCTTT CCTATTAAAA AAGAAGTCTA CATGATTATC TCTATGATAA 2820 AACTTTATCT TTTCTATAAG GAAATCATTA CTTTTAATAC CAGCTCAATT TAGTTAGCTC 2880 TAAATCGATA GAACAATGTT TCCCCTAGAA GAATGAATTT 2920
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