Tag | Content |
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EnhancerAtlas ID | HS076-21451 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr16:12902740-12903910 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2C | MA0497.1 | chr16:12903786-12903801 | TTCTATTTTTATTTT | - | 6.21 | SOX10 | MA0442.2 | chr16:12903239-12903250 | AAAACAAAGAC | + | 6.14 | STAT1 | MA0137.3 | chr16:12903478-12903489 | TTTCCTGGAAA | - | 6.62 | Stat4 | MA0518.1 | chr16:12903475-12903489 | CTCTTTCCTGGAAA | - | 6.67 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 12902743 | 12902971 | chr16 | 12903283 | 12903403 |
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Enhancer Sequence | CTGGGATTAC AGGCGTGAGC CACCATGCCC AGCCTGGTCT TGCCAGAGGC ATTTGAACCA 60 GAGAGACTCC ATCTTGAATA GGGGATGGGT AAAATAAGGC TGAGACCTGC TGTGCTGCAT 120 TCCCAAGAGG TTACGCATTC TAAGTCACAG GATGGACCTT AGGAGGTCGG CATAAGATAC 180 AGTCGTAAAG ACCTTGCTAG GCTGGGCGCG GTGGGTCATG CCTATAATCC CAGCACTTTG 240 GGAGGCCAAG GCAGGCGGAT CACCTGAGAT CAGGAGTTTG AGACTAGCCT GGCCAACGTG 300 GAGAAACCCC ATCTCTATGA AAAATATAAA AATTAGCCAG GTGTGGTAGC AGGTGCCTGT 360 AATCCCAGCT ACTTGAGAGG CTGAGGCAGG AGAAGCACTT GAACCCGGGA GGTGGAGGTT 420 GCAGTGAGCC GAGATCATGC CACTGCACTC CAGCCTGGGT GACAGAGCAA GACTCCATCT 480 CAAAAAAACA AAACAAAACA AAACAAAGAC CTTGCTGATA AAACAGGTTA CAGTAAAGAA 540 GCCAGCCAAA ATGAAGATGG CAATGACAGC AAACCTCTGG ACATCCTCGC TGCTCATTAT 600 ACACTAATTA TAATGCATTA GCATGCTAAG AGATACCCCA CAAGCACCGT GACAGTTTAC 660 AAATGTCATG GCAACATCAG GAAGTTATCC TATATGGTCT AAAAAGGGGA GCTCTCATTT 720 CCAGGAATTC CCCACCTCTT TCCTGGAAAA CTCATGAATA ATCCACCCCT TGTTTAGCAT 780 ACAATCAAGA AATAACCATA AAAATGTGCA ACCAGCAACC CTCAGGGCTG CTCTGCCGAT 840 AGAGTAGCCA TTCTTTTATT CCTTTACTTT CTTAATAAAC TTGCTTTCAC TTTACTGTAT 900 GGACTTGCCC CAAATTCTTC CTTGTGTGAG ATCCAAGAAC CCTCCCTTGG CGTCTGGATA 960 GAGACCCCTT TCCAGTAACA GTCTTATGGC CCCCACCCAG GCACTGACTT TGTGCAAAGA 1020 TGACAACTTC CCCATGATTT CATTTCTTCT ATTTTTATTT TATTTTATTA TTATTTTTCT 1080 GAGACGGAGT TTAGCTCCAT CACCCGGGCT GTAGTGCAGC GGTGCGATCT CGGCTCACTG 1140 CAAGCTCTGC CTCCCGAGTT CACGCCATTC 1170
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