Tag | Content |
---|
EnhancerAtlas ID | HS139-10887 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr11:118560140-118561310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr11:118560527-118560547 | CCCCCACCCCACCCACCCCC | + | 6.09 | RREB1 | MA0073.1 | chr11:118560532-118560552 | ACCCCACCCACCCCCAGCCA | + | 7.54 | RREB1 | MA0073.1 | chr11:118560528-118560548 | CCCCACCCCACCCACCCCCA | + | 8.4 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGTGGGCTGA AGGGCTCCTC AAGTGCCGCC AAAGTGGGAG TCCAGGCAGA GGAGGCGCCA 60 AAAGCGAGCA AGGGCTGTGA GGACTGCCAG CACGCTGTCA CCTCTCAGTG GGGGCTGTGG 120 GCTCTCTTCC CAGGGGCACT GGCCCTGCCT AACCCTAGCG GTACAGGGAG CACCAGTCAG 180 CTCCTCCTCC AGGCCCACAT GCAGGTGAGC ACACTGAGGC CTGGGGCGGG GATCGTGGGC 240 AGCAGAGCCC AGGAGTTTCC TGTAGGGTGA TGGCCAGCCC ACCCCTGGCC TGCTCACCTG 300 AACTTCATAC TCCCCTCCGC CACCGGGCTC TCCACCGTTG CTAATGTCAT ACTGGGAATA 360 AGAGGGCGGG CCGTAGGTCA GGCACTGCCC CCACCCCACC CACCCCCAGC CACAGGGACA 420 ACAAACAACG GGATCCTTGT CGGGAGAAGC CGCTCTGCCT CCCAGCAGCC CCTGCAGTGC 480 CCAGGAGTGC CCACTGGGCG CCGCCACCAT CCCAGCTGCG CTTGCCCTGA GCCCTGCCAA 540 GCCTGACCCT CCCGCCTCAC CACGGGGACG CCCTGGGGGT ACGGGGAGGG CTCAGGCCAG 600 CTCATCTTCT CATACATGGC TGACTTGCTG GTAGACATCA AAGTTGGTTC GGATCCAATT 660 CTGGGGCATA TTGGTAGATC AGGATCTGGC TGCCCTAGAA GGTTCCAGAC ATTCCCGTGA 720 CTGTGGGTGG GGCTGGACTG GGAGCCAGGA CGCTGGGCCC GGCGGGAAGC CAGATGTCCC 780 TTTCCTGGCC CTTCTCTTCT CGGCTCACAG CTGCCCCCCG GTGGCTCCGC GGGACCTGCC 840 GGCTGGGACA AGGGGCACAG CCGGAGGAAG CGGCCTCCCC TGCAGGTCCT GCTCAGGGTC 900 GGGAGGGGGC AGTGCTGCCT GCAGTGGGCC AGAGCCACCT TCTGTGCCCT CACCTCCAGG 960 TATTTCAGAG CCTTGTCCGC CACGCCAGGG TCAGAGAAAC ACCCGTTCCA GAGTGGAGTG 1020 AGGTTGGATG GGTAAAACTC CCGGTTCTCC TTGTTCTCAA GGTCGTAGTC GAACCAGGCA 1080 CTGGTCTGCT CATCCCACAG GACTGTGTTC AGGGCGGCCA AGCGCTGCGC CGGCAGGATT 1140 CTGTACTTTG TGGCCTGGGA GTCGTTCCCT 1170
|