| Tag | Content |
|---|
EnhancerAtlas ID | HS183-01085 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr11:134430500-134431590 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr11:134430731-134430752 | ACCCCCTCCTCCTCCTGCTTA | - | 6.39 | | ZNF263 | MA0528.1 | chr11:134430725-134430746 | TTTTTTACCCCCTCCTCCTCC | - | 7.45 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ACTAACCTTC TGGCCAATCT CAGTTTAGAT ACCCTGCAAT TAAACAAATC CACAAACCCG 60
CAACACATAT TTACATCTCA TTAGCAGAAG CCAAATGCAA CAACGGCATT AAAATTAAGA 120
AATGAGGCAC AATTATCCCG TCGGCGGCAG TGGGGAAGCC GTCAAGGGCT GGTTTCTTCA 180
TTAGTTTGCT CAGAAGTTCA GCAGCTCCCT AATTGTGGGC TGCTATTTTT TACCCCCTCC 240
TCCTCCTGCT TAAAAAAAAT TGTCTGAGGT TTTATTTTTC TGCAGTGCAG CAGCTTCGAT 300
GGGGGGGGGC CAGCAGGGCC CAGGAAGCTT GGAAGAAGTG CTGTCTCCTC TCTGGCCTCT 360
GTAACCTCAG CCCCCAGCTG GGCCTGGCTG AGTGGCAGTG GCTGGGGGTT AGGAAGGCCT 420
GGGGAACACC GGGTGGTGGT GCCCACAGAT CCCAGTGGAC TCCCAGGGAG GGCTCTCGAC 480
CGCTCACAGC CTGTACTGCT GCCATGGGGC TGGAGCTCCC TGGGGCCAGC TGCATCTCAG 540
GAATGCATCC TGCTTCCCTT GGGCAGGCAG CTGTCCCAGG CACAGCTCTC AGGCCGGCTC 600
TGCTGGCCCT CAGTGGGCCT TTCAGGAATG TGTGTGGGGT GGTGAATGAG AATGTTCTGG 660
TCATAGCCCT TTAGTGCAGG TGAGGGGGGA TTCGTGGGGC CCCAGGCTGT GCCCAGGTGG 720
GTAGGCTTGG GCTCCAAGGG GGGTTGAAGA GCACTGGCCA GCTCCAGGGA GAGGCTTTGC 780
CTGGAGCGCC CTCCTTTCTG GAGGGAGTCT TGTAGTGGCT GGCACTAAAA TTGCACAGAG 840
CCTTGGTTTT CTCAGCTGTC AAATGGCATA AGTGAGACAC CTTCCTCCTC CCTCAGGGCT 900
GCGTTTTGAG GTGCTTTGCG AGTGTCCAGG CTTGTTTTAT TGTTGTCCAG CCTCTCGGTC 960
CCCACTGGGA AGCCTGGGCG CTCTCCAGGG CAGGCCCGTC AGCTGGGAGA GCAGGGTTGG 1020
TCGGTGCCCT CAGGGCGGTT TGCCTCTCCC TATCAAAGTG GAGGTTTCAC AGGCTTCCAA 1080
GTTACTGAGC 1090
|
