| Tag | Content |
|---|
EnhancerAtlas ID | HS139-49241 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr6:161795990-161797420 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr6:161797231-161797251 | GGGTGGGTGTGGGTGTGGGG | - | 6.27 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH06I161375 | chr6 | 161796033 | 161797232 |
| Enhancer Sequence | TCATTTTCAG AGGAGGGTCC CATGTGTCAG GCCAGGCAGG CATCTGGTGG AGGCTGCACT 60
GTGGCCGTGC AGAGGAAGAC TCAGGGGACC CGCAGGCTGT GACCCCTACA GGTGAGTGAG 120
CTCAGGGGAC CCGCAGGCCG TGACCCCCAC AGGTGAGCGA GCTCAGGGGA CCCGCAGGCC 180
ATGCCCCTCA AGGCAGAACT CCTGGGGGTG GAGGGAACCC CCCGGGGGTG CTGAGGCTCC 240
TGCAGAGGGA GGACGCCCCT GGCCGGAAGC TGCACCCCAG GGAAGTGCGT TGCAGAGCCT 300
TGGTGCTCTG CCGTGCTGGA GTGACAGTCC AGAAGAGAAG AAGGGTTTCT GCAGTGCAGG 360
AGAGCGCTTG GAGAGCCCCA GCCCCAGGTC TGCATGGTCA GGATCGGCCT CCAGGGGCAG 420
GCGTGTGGTG TCACTGTGTG TGTACCCACG CAAGCATGCC TTCACTTGTC TTTCAATCCC 480
AGTCAATCTT ATCTTTCCTT TCCTCTCTCC ACAGTGCCTG ACAGTTTTAG CATTCAGCCT 540
TAAAAACCCA AACCCCCAAG TTTCACCATT TTGTAATACT TTGCAACTTA CAAACGGCGA 600
AACACACACT CATTTCATTA TTTATAGCTT GGTAGATCTT ACTGGCTCTG TGTGGCAGGC 660
GACGAAAAGG CTGTGAGCCT TTGAGCAACT TGCCTGGAAG AGGAGGAAAT GAAACCGGGC 720
CTTTGACGAC CTGCCAAGGG CCATTTCTGC TGCCCCAGAG CAAACCTTCG CACACAAGCT 780
GAGTGCCTTG GAAACGCACT GCAGAGGGGC GGGTGCTGTC CTGGCACTGA CTCAGCTTTT 840
CACAGCGCAA GGCCGAGCCC GAACGACGCG CTGGCTTTAA TGGAGATCTG TCGCAGCCGT 900
TCCATCCCAT CTGCACATCC ACTTAGGCGG CGGGTCCAGG GTCATGGATT CAAGAGAAGT 960
GGCATCAAAC CTGCTTTACT TAAACCAACA AGCAGTTCAG AAAATACACT CCCAAATAAC 1020
CGGGGATCTA GATCTCCGGG AATAATAAAT TACACCCATC TCCCAATACT GGGACTGCAT 1080
TTGTGTGTGA AGGCAGTCAA TGGCTGAGAG ACGGCTCTGC GGTGAGATGC TGGGGCAAAA 1140
TAGATCAAAA AAGATCTCAG CTCCCTGGAG CCACTGCTGC TTCAGTGTCC TCCACTGAGG 1200
GAGGTGCACC TCCTAGCCTC TCCTGGACTG TAACTCTGAA GGGGTGGGTG TGGGTGTGGG 1260
GAGCATGGAT AAGGGGCAGT TCGTTGGAGA TTGTCAGTCT TGCATCTTGA TCGCTGGCTC 1320
CAGCCTGGAT TCTCCTCTGA GGTGGTCTAG GCATCCACTC CTTTCCCCAC TGAACCCCTA 1380
GCTGAGATGT CCACAATGAA TGTGTGTCTC CCCGAACAAC CTGCTTTTGT 1430
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