Tag | Content |
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EnhancerAtlas ID | HS139-29497 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr2:96980440-96982680 |
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) |
Nfe2l2 | MA0150.2 | chr2:96981424-96981439 | TGCTGAGTCACTGGG | - | 6.54 | ZNF263 | MA0528.1 | chr2:96981951-96981972 | CCCTCCACCCCCTCCTCATCC | - | 7.95 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 96981121 | 96981515 | chr2 | 96980846 | 96982152 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I096314 | chr2 | 96980654 | 96982696 |
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Enhancer Sequence | GGTACCCAGG CTGGAGTGTA GTGGCACAAT CTTGGCTCAC TGCAATCTCT GCCTCCTGGG 60 TTCAAGTGAT TCTCCTGCCT CAGCCTCCCA AGTAGCTGGG ATTACAGGCA TGGGCCACCA 120 TGACCATGCC CAGCTGATTT TTGTATTTTT AGTAGAGACG AGGTTTCACC ATGTTGGCCA 180 GGCTGGTCTC AAACTCCTGA CTTTCAAGCG ATCTGCCCAC CTTGGCCTCC CAAAGTGCTG 240 GGATTACAGG TGTGAGCCAC CATGCCCGGC TGTGTTTAAG TTCTTATTCA ACTAATACAT 300 GTCACTTTTT GTACATGTTC AGGAGTGTGA TGTAGTCAGA ACTGCCTTAA TTTCTTTGAC 360 CAACTCGAAT GATTATATAA TTATTGGCAT TGGTTGAGTT TATTATGTGC CAGGCATTTA 420 ACCTATTTTA TTCTTCAGCA CCGTCTGAGG TCAGTGTTGG GAAAGGCAAT CTGCATGGTC 480 CAGAGCATGC CTGCATGTTC TTGCTGGGTG TGCCAGGAAT GCAAGGCCCT GGCCACACTT 540 TCCTAGGCCC TTTCCCAGAG CTGTATGTGT AGTGGGCAAC CTTGAGGGAT AAGGTAATGT 600 CTTCCATCAG GACAAAGAGA AGAATGGCCA TGAAATAGGT AGTTTCCCTG AAATCAGAAT 660 TCCTTGTCTG CAATGCAAAC CGTACCATGC ATAGCATCCA CCTGGGCCTC TCCATGTTGC 720 CCCTGTGGGA CTTGAGAGAG CAAGGAGAAT TGACACAAAC AGGATGCTAG TGCTGATTGT 780 TGTGCCATGA GTCATAAATT ATTCTGTCTC TGACCCAGGA GTCTTGTGTC TTCTGCCAGC 840 ATCCATGAAA CAGCAACAGT AACTATCTTT TAAGTAGGGT AAAATTCCAG ACTTTTGACA 900 GTTTGGATGG AAAGGATTTA ATGTTGTCAT AACTATGGGG CAGCAAGCCT TGCAGCCACA 960 GCCAAAAGGC AACATGATTG TGGGTGCTGA GTCACTGGGT CCCTAAAACT GAGACAAATG 1020 GCATCAGCAA TGAGGATATA GAGCTTCCAG TGGACCGAAA GCACTGGAGC GTGCAAAATC 1080 TTGTTTATTG GAACAGAGCT GCTCTCTCCC TTTGTGCGAC TGATTCTTTG GACCCCTCCC 1140 CAACCTCAGC TATGTTAAGG AAAAAGCTGA GTATGTTGGG GAACTTCACG GAAGGGGCTT 1200 TGTTACAGGA ACCCAAGTCA CCATCCTCCC CGGTCCTGTG GCAGGAAGCG GTGCTAGGCG 1260 CAGCTGGAGT GGTTTTAGAG CAGCCTGAAA TAAAAGACAC TCAGTCCCTC AGGGCCAGAA 1320 TCAGAGGAGG CTGTGGCCAG AAAAATCCCA GCTACTGGAT GAGCCTGAGG ACAAAGCCTA 1380 GGCAGGCAAA CACAGCCAGA AACTAAAGGG CATCACAAAC AGGAAATCTG ACGCTGGCAA 1440 CATAAAGGGG TCACCACCTC AGTAGAAGCA GGGACCAGAG CCCTTCAAGA GTGAATAGAT 1500 GGACACACAG ACCCTCCACC CCCTCCTCAT CCACATGGAG GGAACTCCAC TCCCTCTACA 1560 ACTCAGGGCC CCAAATTCTA CATGGTTTCT GTGGAAGCAA GTCCTCATGG ATCTAGTTTT 1620 AGTCCCTGGA GAGCTGGTCT CTTGGCCCCT GGATAAGGTG AAAACCTGGT AGGCACTAGA 1680 AAAGACTGCC CTTCCCTTGT TCCCCGCTAT TTGTCCTTCC CATTCCCACT TAGTTCCTTT 1740 GTCTTTTCTC CATTCTACAT GCTCTGTCTC AACGTGGGAC TAAAATATAT ATTGTTATTA 1800 GTTACAGGGT TATTGATTAA GTTTTGGTTT CTAAACTTGC TCTTAAAATG CAGTTGCATT 1860 GAACATTTGA TTTGCCTTTC TTTATTATTA TTATTAAGAC AAAGTCTCAC TCTAACCCCA 1920 GCTGGAGTGC AGTGATGCGA TCATAGCTCA TTGCAACCTC CAACTTCAAC TCCCGGGCTC 1980 AGGTGAGCCT CCTGCCTCAG CCTCCCAAGT GGCTAGGACC ACAGGCACTC GCCACCATGT 2040 CCAGTTAATT TTTTAATTTT TATTTTTGTA GAGATGTCAG GGAGGGGGGT CTGGCTATGT 2100 TGCCCAGGCT GGTCTCGAAC TCCTGGGCTC AAACTATCCT CTGGCCTCAG CTTCCCAAAG 2160 TGATGGGATT GCAGGTGCAA GCCACCCTTC TGACTTGTCT TCCTTCAGAA AACACTGAAT 2220 TGCTTGGTAC TATCTGGGTC 2240
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