Tag | Content |
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EnhancerAtlas ID | HS078-08063 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr18:10725660-10727920 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr18:10727782-10727795 | AGGAGCAGCTGCA | - | 6.15 | RREB1 | MA0073.1 | chr18:10727233-10727253 | GGGATGAGGGTGGTTTGGGA | - | 6.03 | RREB1 | MA0073.1 | chr18:10727036-10727056 | TCTTGGGGGGTGTTGGGAGG | - | 6.1 | RREB1 | MA0073.1 | chr18:10726124-10726144 | GGGTGTAGGGTGGTGGGGGG | - | 6.36 |
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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 |
GH18I010726 | chr18 | 10726399 | 10726663 |
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Enhancer Sequence | TCGCCTTCAT CTCTTGGTCC TTTCGGGTAT ATTTTTCTCT CTCCACTTCC TCTCCGACTT 60 CTCTCCACAG TGGCGGCAGG GCTGGTGAGG CCCTGACAGG CCAGAGGGAG AACGCTCAGG 120 GTCCCACCAG GCCAACCACC ACGCGGGCCC TCCAGGGTGG ATGGAAGGCC AGATCCTGGG 180 AATGGACTTG GCTTGAGGAC ACACGGCGCC TGGTTTAGGA GGCGACTGGC CAGGCTGGGC 240 AGGAGGGTGC AGGGCACTAA CCACTATTTC TATCTGTCTG TCCCTCTTCA TCGAGAATCC 300 TGTTGCTCTG GGCAAGAGGT GGTTTTTACC GAAGGCATCA GCGTGACTGT TCAGAATAAT 360 ATGGGCACCC AGGATGTTGG GCAGGGTGGT ATATGTATTC TTGTGTCCAG GAGGGCTGGG 420 GGCAATGTCA GTTCGGGAGA GTTCGTGCAC GTGTGTGGGT GCGTGGGTGT AGGGTGGTGG 480 GGGGATGGGT GGGAGAGGAT TCATATATGT GAGCAACTGT GGATCCTTGG GTGCGAGTCC 540 ACCGGAGGAG GGGCTTCACG CTGCCTGGGG CTGGAAGAGC TTGTGTGCGA GCCTGTGTTC 600 GGGAGCATGA GAATGGAAGC GTCGCGGCCA GAGCCCCGGC CAGGTGGAGC AGGTGGGTCC 660 CCGAACGCCC CGCCCAGCGC TGCCTCCCTT CGCCTTCCCC GCAGGCACCC ACTACCTGCG 720 GGGCGGTAAC AACGCGCGCC AGCCGTGGCA CAACGCGGAG GGCCGGCTGC GGTACGGGCT 780 ACGGCCGGCG AACCCCACGA GGAGGGCCTG GCCACCCTGC ACAGCGTGCT GCTCCGCAAG 840 CAGCCGTTCC TGTGGCGCGC TGCGCTGCTC TGCTCTGCTA CACCAGCCGC CACGCTGTGC 900 GTCTGTCCTT CCGCCAGCTC TTCCAGGACC TGGCGCGCTA CGTGCGGGAC GCCGACGTGC 960 GCTGGGAGTA CTGCGCGCGC GCCAAGCGCG GCCAGACAGA CACCTCGCTG CCAAGTTAAT 1020 TCAGCAAGGA CCAGGTGTAC CTGAACGGCA TCCTGTGCAT TCTGGGACAT CGCCAGACCA 1080 TCGATTTCCC GCTGCTGACC TCACTGGGCA AGGTGTCCTA TGAGGATGTG GACCACCTGC 1140 GGCCCCATGG GGTGCTGGAT AATACCCGGA TGCCCCACCT TATGCAGGAC TTGGCACGCT 1200 ACCGGCAGCA GCTGAAGCAC ATCATGGCCA CCAACCGGCT GGATGTGGCG GAGCTGGGTC 1260 GCCTGCTGCC CGACTGATGT AGGTTGAGGG CTGCAGACAG AGGCCCTGGA CAGAAGCTCC 1320 AGATAGGCCC CCAGAACATG AAGCTGTTTG CTCTGTGCTT CCACGGTCTG GGTGTTTCTT 1380 GGGGGGTGTT GGGAGGGCAG GAGCATTCCT TGAGAAGGAG TGGCAACATC AAAGGGTTTG 1440 TGTCCCTTGC TAGCCTCCCT GGGGCCTGGG GATCTGCAGC AGCATGTCTG GCAAACTGAG 1500 TCGCCCTCCT GCCTCCAGCT CTGTGTTGAG CAGAGGGAAG GCATGGGGGC AGGAAGGGAG 1560 CTGAGCATTG ATGGGGATGA GGGTGGTTTG GGAATAGAAA CTTGTTCTTG CATAAGATGG 1620 CTTTGGTTGT CCCGGTACTC CAGTCTCTCC CTTCCCTCAC CTGTCCCCTT GGTGCTCCTT 1680 CAGCATTCGT GCTGTCTGCT TCTCACTGGG TCCTGGTGGG GGTCGGGATC CCTTCTCCTG 1740 GGGTGATTGA TGGCCTGAGC TTGGGGTACT ACCTGGGGTA GTAGAGACCC AGTTGGTCTG 1800 GGGTGTGCTT TCCAACATTT TGCCTCTCTC ACTGGTCATG TATTTATTCC ATATTTATAT 1860 GATCTACTTC CTGTGGCTGG GAGCAGCAGC TCCTGAAGGT TCCATGGCAG GGAACAAGAC 1920 ACTCCTTCTG GAAGGCACCG ATTTTCCTAG CCCCACTCCC ATTACACGCA CACACACACA 1980 CACACATACA GAGTGATTCA GGCCTTGTGA ATCAAGCCCA AGAGCTCCCT TGGCCCTGTC 2040 CCCACTCCCT CCACTGGCCT CTGCTTTTCC TGTCTTTGCC CACACCCTCA CAGCTGGTCT 2100 CTGGCACAGG CTGGCATAGC CTAGGAGCAG CTGCAGTTGT CCCTGAGGGA CAGGCCCTAG 2160 AGTTTGGTGG CCCAAGTCCT AAACCCCTCC TGGACCAGGT GAGGTGCAGA GCGCCTTTTG 2220 TGTAAGTTAC TGGTCAGAAT CCTCACTGAG CTCCCAGTCC 2260
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