Tag | Content |
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EnhancerAtlas ID | HS112-00270 | Organism | Homo sapiens | Tissue/cell | KELLY | Coordinate | chr1:35411010-35412620 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr1:35412413-35412425 | TCTATTTATAGT | - | 6.22 | MEF2B | MA0660.1 | chr1:35412413-35412425 | TCTATTTATAGT | - | 6.37 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTTCTTGCAT CCTAGACTTT CATTCTGAGG TATTATAAAA TCTCACAAAG GTTTGGGTGC 60 AGGGGCTAGT TCTGAGTAGT CCCAGCTACT TGGAAGGTTG AAGCAGGAGG ACAGCTTGAG 120 CCCAGGAGTT TGAGGCTTCA GTGTGATATG ATCATGCCTG TCAATAGCCA CTGAACTCCA 180 GACTGGACAA CATAGTCAGA CTCCATCTAA AAATATAAAA AATAAAAATT TCATAAAGGT 240 AAGCAGAAAT CTCAAACTTT CTGAGATTTT TCTTTTCTTC TTCTTCTTTT TTTTTTTTTT 300 TTTTTTTTGA TACAAGGTCT TGCTCTGTCA CCCAGGCTGA AGTGCAATGG TACAGTCTTG 360 GCTTACTGCA ACCTCCTCCT CCCAGGCTCA AGCAATTCTG CCTCAACTTC CCAAGTAGCT 420 GAGACAACAG GCACACACCA CCAGGGCCAG CTAATTTTTG TATTTTTTGT AGAGACATGG 480 TTTCACCATG TTGCCCAGGC TGGTCTCAAA CTCCTGAGCT CAAGTGATCT CCCTGCCTCA 540 GTCTCCCAAA GTGCTGGGAT TACAGGCATG AGCCACCATG CCTGGCTAAC GTAGAATTTT 600 TGCAAGCAAG CAAAATGTGG AGGCTTTAGG CCATGGCTAG CCAAGCCATA AATCTGCATA 660 CTCAGAACCC AACCATTCAG GGAAGGGCCT CTCCACAGTG GCAGTTGACT CCAATCATTG 720 CCATGTGCCA TTGTTAGTGG AATTGAAATG CTGCTGCTTT GGCTTGATGC CTGAGATTAA 780 AGTTATCTCT TGTGAAATGG AGAGAATGAT TTTTCTGTGT TATGCTCAGT TGGAGAAGTC 840 CTGCAGTGAA ATTGCCTGAG CTGTTAGTTA TATGGCTCTT TTTCTCATTG CCATGGACAT 900 CCAGGCAGGG ACTCCATAAC CTCAGGCCCT AATAATTTCA CAAGAGTCAA ACTCCTGCTG 960 TAACTCTATC CCTGCTGATG TTATCACCAC CACCACCACT ACGAACCAAT GAAGCAAGAA 1020 CGCAGCCATG CCACATGCAG GTGGAGCGGG AATTCGGCCG TAGCCTGAAG GCCATGGAAC 1080 TTGGAGGCTG CATTGCATTC AAGGGAGAAG GTTTGTGTTT TTGCTCCTTG GAAGTAAGAA 1140 AGAGATGCTC CCTTTGAGGA GTACTCAGTG GAAGAGAGGA GGGGATCGTA GTAAGGTTGA 1200 CTGAACCTCA TTACGTTTTA GAGATCAGTG GTTTCATTCT TTCAACTCAA ACTCATAACC 1260 CATGTCTCCC AGGGTGCACA TCTACCACTG GAGTGACCAA ATTTAAATTA TCTCCAGTAT 1320 CAGCCTCTGT CTTACACCTG GAACCAGCAC TCCGTTCCAT TACTTACGAT CTATTGCTAG 1380 AGTTGGTTCA TGTGCCAACT CCTTCTATTT ATAGTGAGTC TCCCTCACTG ACTTCTGATC 1440 TCCTTCTCTG CCCGCCGGCT TCTGTTGGGG TCACCCGCAG TCCATAGTCA TATTTGTATA 1500 TGTCTGAAAT AGGTCAGGAC TTCTCTTCAG AGATTACTCA GGTCTTATGT AAATCGTAAA 1560 TACAAATGGA TACAAAGGGA AGAGATTTGC CTAACTTTTC TCCGAAAGAC 1610
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