| Tag | Content |
|---|
EnhancerAtlas ID | HS007-10397 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chr20:62777290-62778730 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr20:62777919-62777930 | GACAGCTGCTG | + | 6.14 | | Tcf12 | MA0521.1 | chr20:62777919-62777930 | GACAGCTGCTG | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCGAAATGTC TCCCTCCATG TCCTGCCCAG GCCTGCTCTT TGGGTCTCCT GGCTGGTGGG 60
GGAACAGATG TGGCGTAATC ACGTCGAGAT GCAGCAGGTG CACCAAGCAC TGTGCGCACC 120
GCTGTTAGCC CCAGGACCCC CAGTGTCAGC ACTGGTGGGG CTGGTGTTTG TGGAGTGTGT 180
CAGTGGACTG GCAGGCCCGT GGATTCCACG TGTGTAAGAG AGACTGACAG CCCTTCCTGT 240
CTCAGAGCAG CCCCTCCTGG GTCCCATCCT GGGTCCCATC TTGGGGTTGG ACATGCCCTT 300
GTTTGAGCTT GGCCCCTTCT TGCTGGGCCA CCAGCCCTGA CCCTAAATCT GAGAGGGGGC 360
TTGGCTGGGC CTGGGGTCAG GGGACAAACA GCCACCCTGG CTGAGGCCCT GGGCAGCTGA 420
GGAACTTCAG CCAGCTTTGG GCAGCTCTTG GGTTGGGAGA TGGGCTGCTG TTTTCTCGGA 480
CAACGCCCTC CCCAGCCCCT CAAGACTCTG TTTTCAGTCA GTTCAATTAG TACAACTTTA 540
AAGCAATTAG GGAGAATTAG TGGCCAGGCT GCTGCAGGCA GATGCTGAAT ACACTCATGC 600
CCCCTCCCCC AACCTCCCTC ACCGAACCTG ACAGCTGCTG CGGGGAGTGC CTTTCTCTGC 660
TGGCTCTGTC CTTTCTCCCA GAGATCCAGC CCCCATCTCT CCTTCTCTCA AGGGTCTGAG 720
GAGGGGAGGG TGGGCAGTCT AGGGGACAGA CCCAGAGACA GGGGCCCTGG GACTGGGAGG 780
GTGGGGCAGG CCCGGGGAAA TGGGCCAACT TCCCCTCAAG ACCCCAGGCC TGGGCCTGCT 840
CTAAGGAGAG AAGGGATGGG TGCTGGTTGG AGGCTCAGCC CCTGAGTGAG GGTGAGGGTA 900
CTCAGCGCGG ATTGGGAGGA CTGACCAGGA TTGTGGCCCA GCCTCTGGCC CTGTGGCCTC 960
CAGGAGCCCC CAGCTCTGGT GAGGGCACCC TTTGGTGGGG CTGGGGGCTG TTCTTCAGTG 1020
GGAGGCCTCT GAGAGGCTGG GCCTCTCCCA CTAGGTGTGG GGTGGCAGCG AGGCCCTGCT 1080
TCTGAGCCAG TGCTGGAGCC ACACCACCTT CTCTGCCTGG TAGTGAAGGA GGTGGCCCCG 1140
TGGGTGCTGC AGACCCTGGG CCCTCCCTGG TGCCCCTTGG GCTGCTCTGT GGGGAGAGCT 1200
CCAGGTGCTT GCTTGCGTGG ATGGGGCACC AGGGCAGGTG CAGGGCTGAC TTCGCAGATG 1260
GAGCCCTTTG TGCGGGGACC CTGTCTTCCG GCCTTGCCCC TCCCTACTCC CCCAGCTTCT 1320
CAAAGAAGGT CTGTTTTCTG AGCCTCCTCT GTGATGCCCC CACCAGCCGC AGCCTCCCTC 1380
AGATGTGTGG GGGGTGTCCG CGGTCCTAAC CAATGTCTTT TCTGCATGTG TCCACGTGTA 1440
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