Tag | Content |
---|
EnhancerAtlas ID | HS120-00378 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr1:116253720-116254380 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr1:116254263-116254275 | GTTTGTTTGTTT | + | 6.32 | SOX10 | MA0442.2 | chr1:116254275-116254286 | TGCTTTGTTTT | - | 6.02 | ZNF263 | MA0528.1 | chr1:116254169-116254190 | TCCTTTCTCTCCTCCACCCCC | - | 6.07 | ZNF263 | MA0528.1 | chr1:116254014-116254035 | TCCCCTTTCATCTCCTCCTCT | - | 6.83 | ZNF263 | MA0528.1 | chr1:116254163-116254184 | TCTTCTTCCTTTCTCTCCTCC | - | 7.41 | ZNF263 | MA0528.1 | chr1:116254166-116254187 | TCTTCCTTTCTCTCCTCCACC | - | 7.4 |
|
| 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 |
GH01I115713 | chr1 | 116253961 | 116254110 |
|
Enhancer Sequence | ATCTGTCCTC ATGGCCCCAC TCCTGGGGGA GCTGGCTGTG CTCACTCCAC AAAGGCACGG 60 AAAGGGACCC TTCCTGACTC CATGCCATGG GAAGTTCTGG GCCTCAGGGT CTCTGCTCCT 120 GTGAGGAGAG GCCTGAGCTT GGGAGGGCCA AGCTCTTAAA GTGGGGTCCT GCCCTTGCTT 180 GTGTGGCAGG TGGACAGATA AACGGCCGGG GCTGGAACCA CACAGCTTAG AGGTTGTGTC 240 TAAAGAGGGC ACTGGGTCTG GAGTTTAAAG ACCTTGCACA GGTTGCTTAA CCGCTCCCCT 300 TTCATCTCCT CCTCTGAAAG TGGAGAGAAC AGCTGCCACA TGACTTCTCA GGCATGTTGA 360 TATAACGAGA TGCTATCAGC ATGTGGGTTG GGCAAAGTGT GTAGGGAGAC ACATGCAGAA 420 GGTCCTCATA AAGACTTTGT CTGTCTTCTT CCTTTCTCTC CTCCACCCCC ATCAAACTCT 480 TACTCATTTT AAGATTTTTT TTTTTTTCAC TACTTTGATC CTTCGTTGAT GGGAAGGGTT 540 TTTGTTTGTT TGTTTTGCTT TGTTTTTGTT TTTGAGATGG AGTCTCACTC TGTCACCGAG 600 GCTGGAGTGC AATGGTGTGG TCTCGGCTCA CTGCAACCTC TGCCTCCCGG GTTCAAGTGA 660
|