Tag | Content |
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EnhancerAtlas ID | HS069-04940 |
Organism | Homo sapiens |
Tissue/cell | GM18951 |
Coordinate | chr2:171828840-171831100 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr2:171830100-171830119 | GGGCCACCAGGTGGCGCCG | + | 7.85 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 171829059 | 171829400 | chr2 | 171830600 | 171831100 |
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| Number: 2 | ID | Chromosome | Start | End |
GH02I170972 | chr2 | 171829111 | 171829310 | GH02I170973 | chr2 | 171829415 | 171831716 |
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Enhancer Sequence | CTCTGTCTCA AAAAAAAAAA AAAAAAAAAA CCTTGTTCCA TCTCTTCTGA AGCCTTTCAT 60 TTCAGTCTGT CCAGGACGGC CGCTGCTGCA GGGCCGGGGA AGCTTTTTCC CCAAGCAGCG 120 TCATGACTGG TCAGACTAAG GGAGCTCTCT GCTAACAACC CCCAACACTG TCCCTAGATT 180 AGAATTATCC ATGAAATTTC CCTGAATAGA CTTGCACTGT GACTGATTTG CAATGCTGTG 240 TTGTGTTTGT AAATCAGTTT GGCCAGAACC GTGTAGCTCA GACAGCTATG CTGAAAGAGC 300 CCAGAAACAC AATGGCAAGA ATCCATGTTG TACCCAGGCG CTGTTTTGGC TTCTAGAGCT 360 CTGGAAACAG TGTTAGCGTC AGGTAGTGAA GTATGCATGG TTCCAACACG TTCACTCGAG 420 ATCAGTGGCT AAACAACCTG TGTGCTTCTC GGTGGTGAGG AACAGAACTG CTAGAGGAGC 480 CTCATAAAAT CAAGAAGAAA CAGATGCCTG TTGTATGAGT CCAGGAGCTC AAAGCTCATT 540 CCGATTTTAA TAAACAGTTA CTTGCCTTTG TCTCTGTCAA GGTTTTGTTT TTAAAGGGCA 600 TGAAACTTTA GAGACTAATT CATTTCCCCA AATTCAGATC TCTCTTAGGT AAGCAGTACA 660 ACCTGAGAAA AGAGGACAAC CCTCTGGGAT CTTTGGCACC GTGACGCTGC CATATTCCAG 720 GAGAGGACAG GTGAGGGTTC GCTGTGGCTG AATCGGAAGG AGACAGAAGA AGCAGGGACG 780 AGCCACCGGG CAGGCCTCAG GACAGGCTTA GGTTCTGAAC TTGATCCCAT GGACTGGTGT 840 TACCCAGAGT GAAGAAAACT GTCTTTCCTC CTTTAATACC TATATATTTT ATTTTAGCAC 900 GTATTGGGGA AAAAATAATA GTTGCATTGG ATATGGCTAA TTTTACGAAT TAACTTCAGT 960 GAAAAAAGGG AATGGTTTTA AAGAGAAGTG ATGGGTGAGT TCTTGAGTTA ATTCCCTCAG 1020 GGGAAGCAGG TGCGCCTGGA GAGCTCAAAC CGAGGCCCCT GCTTCACAGG CGGGCGGGCT 1080 TTGGGGTAGG AGCTGAATCC ACGTAGGTCT GCCCGGTCCC ACGCCTCAGT TCTGTCCCCA 1140 CGCGGCAGGT TCCTGGAACG ACATTCACCT TTGTTCAGGA ACTCCGGTCT TACCGCCGCC 1200 CACGTGGAGT GGGATCCGAG CCAAGGGGGC CTCCCGAGCG GGGACTACAG TGCGCGCCAC 1260 GGGCCACCAG GTGGCGCCGG GAGCCTGGGA AAGCCGCGCC CCGCCAGCGG CCGCGGGGTC 1320 TCCGGGCCGC CCTCGCAGGG CCCCTGGGCG GGGCCGGGGC GTCGCGGTGG GGCGCTTTCC 1380 GTTCTTTGGA AGAAGGGCTC TGGTCCCCCG CTTTCTTTCC ATCTCAGACC CAGTGCGGAA 1440 ACGTGGGGGA TGAGCCTGGG CGCCTTCACC AAACGGAACC CCCTTTAATC TGATGTGAAG 1500 GCAAATCTCT CCACCGGGGG ACCCGTTGGG TGCGGCGGAG ACACCCTTCG GTGGCTGAGA 1560 AACCCTCAGA CGCCGTGGAA GCACCAGGGG TCTGAGCGCC CAGTGCGGGA GGTGCGGGGC 1620 CGGCTTCCCT CCCCGGGGCT GGAGCCTTCA GGAGCGCCGC CCCCACCCGG CTTCCTCCGA 1680 GGGCAGTGCT GGACTCTGGC CTGGCCCCTG GCCGGCCGCT GCCCTTGGCC TCGTCCAACC 1740 CACACCCGCG GGGCGGAGGC TCCTGCTGTG CACAAGCCCG GGGCGCCGGG GTGGGGCGGC 1800 TGGGTCTGGG CCCAGGTGTC CCGAATCCAA AAGCATCCCA CTGCGCTGCC TGTAAATTAG 1860 CGATTTCGGA TCTAGTGATG AGCAGAGGGG ACAGAATAGC CCAGAGGCCG GGTAACTAAC 1920 ATGTGCGGGA TCAAGGAAGG CGTTCGTGGG CAGCTACTAT TAGGGCTTTG AAGAATGCAT 1980 AGAGGTTCTC TTAGGTGGTC AAAGTGGAAG GAAGAGGTTC TCTTAGGCAG AGGGAACAGC 2040 GTCTGCAAGG ACACACAGGA ATGTGGCACG TGGTGTGTCC CGGAACTACA AACAGCTCTG 2100 GTTGCTGGAA TGTGAAAAGT CAAGTATGGA GTGGTAGCAG TTGCCACAGA AGGGGGAGCG 2160 GGGCCAGATC GCCGAAGGCC TTGAATGCCA TGCTCAGGGG CTTAGACTGC ACTGCCCTGG 2220 GGAGTTTATA AGGGGGATGG ATGTTTTTTG TTCTTGGCAG 2260
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