| Tag | Content |
|---|
EnhancerAtlas ID | HS183-00663 | Organism | Homo sapiens | Tissue/cell | T47D-MTVL | Coordinate | chr10:47663840-47665060 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr10:47664148-47664169 | GGGTCAGGGAGAGGAAGGGGA | + | 6.01 | | ZNF263 | MA0528.1 | chr10:47664230-47664251 | AGAGGAGAGGGAGGAGGGAAT | + | 6.12 | | ZNF263 | MA0528.1 | chr10:47664218-47664239 | GAGGGATGACGGAGAGGAGAG | + | 6.24 | | ZNF263 | MA0528.1 | chr10:47664221-47664242 | GGATGACGGAGAGGAGAGGGA | + | 6.2 | | ZNF263 | MA0528.1 | chr10:47664142-47664163 | GAAGGAGGGTCAGGGAGAGGA | + | 6.8 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACTTGGCTGG GAATGAGATT AGCTCAGGGA GGGCTGGGAG AGGGCTGGGC AGGTCAGCTT 60
GAGGCCAAAG CCACAGGGGC TCATTATGCC AGGCCAAGGA GCTGGGATTT CCTGCTCTGA 120
GCCATAGAGA GCCAGAGAAG GCTCTTGAGC AGGGGAGTGG CATGATCAAG ATGGCACTTA 180
AGGAAGAAAA GTCTGATGAC TGTGGGTAAA ATGAATGGGC AACAAGGGCA GGAGCCATGG 240
GGAGCTCCGC TGGGGACGTA TGGCAGCACT GTCGCTGAGG GCCACTGAGG GTCAGCCGGC 300
AGGAAGGAGG GTCAGGGAGA GGAAGGGGAG GCTGTGTGCA TGGCTGCCAA TAGGGAGAGT 360
CACTTGTCTG AGATGAAGGA GGGATGACGG AGAGGAGAGG GAGGAGGGAA TGGGGTGAAG 420
AGGCAAAGAA TTTTCCAGTA GAAGGGAGGC CAGCTGGGAG GGCTGTATGT GCATCTCCCT 480
GCCTGTTCAT TATAAGGTAT GTGTGTCTGT GTGTGTGTGT GTGCAGGTGC CTGAGTGTGG 540
GTGCCGTGTG TGCGTGTTCA TATGAGTGTG TGCATGTTCA GGTGCATGTG TGTGGGTGCA 600
TATGTGTGTG ACTGTGTGTG TGTGTGAGTG TGTATGCATG TGTGTGGGGG GGTGTGTATA 660
CCTGTGCGTG TGTGAGAGTG TGTGCGTGTG TGCCTGTGTG TGTGTGCGTG TGTGCCTGTG 720
TGTGAGTGTG TGCGTGTGTG CGTGCATGTG TGTGCATGTG AGTGTGCCTG TGTGTGAGTG 780
TGTGCCTGTG TGTGTGAGTG TGTGCCTGTG TGTGGGTGTG TGCGTGTATG GGTGCATGTG 840
TATGGGTGCA TGTGTGAGTG TGTGTGTATG CATGTGTGTG GGTGTTTGTG TGGTGTGTGC 900
ACCTGTGTGT GTGTGTGCCT CTGTGTGTGC ATGTGTGTGC ATATGTGTGT GAGTGTGTGC 960
CTGTGTGTGC GCGTGTGTGT GTGCAAGTGT CTTTGGGGTG TTGGGAGTGT GGGGATGCAG 1020
TGAGTTGCCA TCCTGACTCT CCCTTCTATG GAGCCCTTGT CTCCACAGGC CTCAGAGTCC 1080
TTCACTACAT TTATCTCACC TCCTTGTGTC CAGCAAGGGG CTCCAAAGCG GAAGAGTTGG 1140
GGTGGGAGGT GGGGAATTGG CCTCACCACC TTGGCTTCTG AGCCTGTGCC ACTGGCTTCT 1200
CACCAGCACA TGATTCCTTC 1220
|
| |
|
|
|
