Tag | Content |
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EnhancerAtlas ID | HS145-15332 | Organism | Homo sapiens | Tissue/cell | NHBE | Coordinate | chr21:42612580-42613740 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr21:42613316-42613327 | GACAGCTGCGG | + | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGGCCCACCC TATAATCCCA AGAGGTGATT TTGTCTCACT GGTTGACCCA AACGCCCACA 60 AGTGTTCTGA CAGAGATTGC ATATGGAAAT CGTGCTAGAT TCTGCCTCGG AATTCTGCAG 120 AAGCTGAGAT GAAACAAGTA GGAGGTCAAA CACAAATGGA CTACACCAAT GGGAAGATCT 180 GTATCTATTC CATGGTGGAG TTCCCCTCTC ACTCCCTCTG GAATCACAGT TTTAGTTCTC 240 ACGGATAGTA AATAATCATT CCTGTGAATG ACCATGGGCA CCCAGGGGAT GCCTATAGCG 300 TCTGTGCTAC TATAGTTAAT TACATTTTCA TCAAAAACTA ACAACTCATG GTCACCAACT 360 CCAGTGTCTC CCAGTTGTCA AAGCCAAAAT CTAAACTCAG GTCTATCACT GACTTCCTAC 420 ATGACCACCG GCACCCCTGG CACACCGGCA CCTCACAGCT GTTTACGGAC CTTCCCGCTT 480 CCCTTTGAGT CTCTCTGGAG AAATGAGGGC ATCCTCTGTA TGTCTTGCTG GATGTGAGGG 540 AGACACAGAG CACACGAGGG CTTCTGAAAT CTGGCCTTGG GGGAATAAGA AGCCTTTTAT 600 GCTTCTGGAG TATAGATTTG TGCCTTTCCT GCTTCTTTCC TGCCAGAGTT CATCTGGCAG 660 AGCTAAGCCT CACCCCAGGC TCTGGGGTCC GGGGGATACT GTCCTCCCAG GTCAGCCACC 720 TCTCATTTGC ATGGTGGACA GCTGCGGCTG ACAGGCAAAC AAAGATGTCT GCGGCCATGG 780 CAGCTCCTAG AGAAACTCTT CTCTCCTTAC TCTCAAATGC CTAAGATTAG GATCCACCAC 840 CTGCCACGGT AACCTACTTC CACGGCTTCT CACACCCCCT CACAAGGCAG TCATGATGAT 900 AGATGTGACT GCGTCGAATG GCTTCCAGAA ATATGATCTT ATTTGTACAA CAGAGCCGTG 960 CCCAAAGGAA GAATGCCAAC CAGTGGGAAG CTCTGCTGGG GCTTTCTGAA TTCCTAGACC 1020 CAATCACAAG CTGGTGTACT GTTGAACCAT GAAAAAATTG AGTATAAACA CCAGGAATGT 1080 CTGTGGCGCG TGGCGTCTAC ACTGGGTGAC CCATGTCTAC ACTGTGAGTC CTAAGCGGGT 1140 GCCCCTCTCT GTCGCCCTCC 1160
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