| Tag | Content |
|---|
EnhancerAtlas ID | HS108-08227 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr11:76905570-76907200 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr11:76906502-76906513 | AACAGCTGCAG | + | 6.02 | | Tcf12 | MA0521.1 | chr11:76906502-76906513 | AACAGCTGCAG | + | 6.62 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TAGAAGGGCT GAGAGGAGTC CTAGAGAAGG GATGTGGACC TGAACAACCA AGGAGGTCCC 60
AGGCCTCATC TGAACCTCTC TGTTGGGGCT GCGGGGGATG GGATGGCACC TTCCAGTGGC 120
CCTTCCTTCA TTGGACATCA GCTCACTCAT TCTCCTTCCA TCTGTGTGCC AGGCACACAG 180
AGGGAATCAG ACTTAACCTT GCAGCCTCTG TGGGGCCATG GGTATTGGGG CCCCTTTCCT 240
GGTCTTGTGC CAGCCCCTCA TTGGTGTTAT AGCTTCCAGA GCTGCAGCTC AGGAGTGGCG 300
GTGGATGCTA GACAGAGCTT TAGGAATTGT ACCTCCTTTT TCCTAAAAGA ACTCCAGCCC 360
AACTTCCCGC CTGGGGAGCT TTAGGGACAG GCCCCCTTGA CCCTCTTGCT TGGAGCCCAG 420
GCCCATGACC AGCCATGAGT GGTTCCCTCC CAAGCTAAGA GCCTGGCCAG GTAGAGCAGG 480
GGTATCCAGA TGGGGAGAAG GTGGGAGCAC TGGCTGCTGG TAGGGGACCC AAGGCCGCCT 540
CATCTCCATG GCCCTGGCTG TGCAAGAGAA TTGCCCCCGT ACATAAGTCG AGGGCTCCAT 600
AGTCTGAGGG CACCACAGAC CCGGATCTCA CCCCTCCACC TCGTGGCCTC CGTCCTCACC 660
CGGGAGCCCT GTGCCACCCT CCACCTGACC GTGTGCCTTC TCTGGTCAGC TCCCCGCCAG 720
CCTCTGCCTC TCCCTGAGTC CTGAGTGCTC CCTGCGCCAG CCTGCTTCCC CCGAGGCCCG 780
AACCCCCCCG AACCCCACTT CAGAGGAGGA GCGTCTCCTC CCTGCCACCC CTCTGTCCCT 840
CAAGTGAGAG CCCTGCCCTT CATCCTCAGG CACCTCCTCT CCCTTGGCCC TCACATGCCG 900
GCAGCCACTG CAGCCTGTCC AGCTAACTCC CAAACAGCTG CAGCCTCCAC CCCCACCTCC 960
CTGAGGGCCT CCTCGGGGCT CACTGCCATT GTGGCATATG GTACGTCCTG GGTGGGGTGC 1020
TATTATTATG CATTCATTTT ATTTTGGGCA TTTGTCATGT GCTGGGCACC ATACCAGGAC 1080
CTGGAGACAC AGCCCTTTGT GGGACAGACA TGGTTTCTGC CCTTTGGAGC CCACAGCTGA 1140
GCTGGGTCTC TCCTGGACTG GAGCTCCTCA GAGTGTCTGT CCCAGAGCCC TGGGCCAGGC 1200
CCCACATAGA ATGGACAGTT GTGAATCACA GTTTTTGTAG GGTGGGAGGG TGCATTGTTC 1260
ATTTTCTAGG TCTGCCATAA CAAAGTGCCA CAGACTAGGT AGTTTCAACA ACAGAAATAA 1320
ATGTATTTCC TTCTAGTTCT GGAGCCTGGA GCTCCGAGAT CAAGGTGTCA GCAGGGGCTT 1380
TCTCCTGAGG CTTCTCCTCT CGGCCTGCAG ATGGCTGTCT TCTCCATCTG TCACCACACA 1440
GTGATGTGTG CACATGCACG TCTGAGTCCA AATATCCTGC TCTTAAAAGG GCACGGGACA 1500
TATTGGATTA CAGCCCACCC AAGATATCTC ATTAGTGACC TCTTTAAAGA CCTTATCTCT 1560
GGGCCAGGCG CGGTGGCTCA CGCCTGTAAT CCCAGCACTT TGGGAGGCCA AGGCGGGCGG 1620
ATCATGAGGT 1630
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