| Tag | Content |
|---|
EnhancerAtlas ID | HS133-28698 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:72771030-72772180 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr7:72771249-72771261 | AAATGTTTGTTT | + | 6.27 | | Foxd3 | MA0041.1 | chr7:72771253-72771265 | GTTTGTTTGTTT | + | 6.32 | | ZNF263 | MA0528.1 | chr7:72771701-72771722 | GGAGGAAAGAGAAGGGAAAGG | + | 6.03 |
|
| | 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 |
| GH07I073357 | chr7 | 72771521 | 72773050 |
|
Enhancer Sequence | CCCCCCCAGC TTGGCCTCCC AAAGTGCTGG GATTACAGGC ATGAGCCACT GTGCCTGGCC 60
CTCCTCTCAT GTCTTATTCA GAGCCTGATG GTGCGGTGCA TGCTTCCAGA ACAGTAGCGA 120
TGGGTGTGCC TCATGACCGT AATGGAGCTG CTGCTCGCTC CACCGTTAAA CACCATGCTG 180
ACTTTGGCTG AGCTGTATTT TTTTCTTATC ATGTTATGGA AATGTTTGTT TGTTTTTGTT 240
TGGTTTGGTT TTTTTTTTTT TTTTTTTTTT GAGACGGAGT CTCACTCTGT CACTCAGGCG 300
ATCTTGGCTC ACTGCAACCT CTGCCTCCCG GGTATAAGCA ATTCTCCTTG CCTTAGTCTC 360
CCAAGTAGCT GGGATTACAG GCACCAGCCA CCACGCCTGG CTAATTTTTG TATTTTTAGT 420
AGAGATGGGG TTTAATCATG TTGGCTAGGC TGGTCTCGAA CTACTGATGT CAAGTGATCC 480
GCCCGCCTCA GCCTCCCAAA CTGCTTTGAT TACAGGTGTG AGCCAATGCG CCTGGCCACC 540
ACCTCAGTCT TTACTTACTT CTGTCCCGTT GCCTGTGGTT CTGGAAGTCT GACTGGAAAG 600
GGGTCTGTTC CTGACACCCC ACCTCCTCTT CCCTCTCTCA GGTGCTGGCT CCTTTGGTTG 660
TATTGGGGTA GGGAGGAAAG AGAAGGGAAA GGGTAGCTCA CGCCTGTAAT CCCAGCACTT 720
TGAGAGGCCG AGGCAGGCAG ATCACTTGAG GTCAGGAATT CGAGACCAGC CTGGCCAACA 780
TGACGAAATC CTGTCTCTAC TAAAAATGCA AAAAAAAGTA TCCAGGCGTG GTGGTGCGTG 840
CCTGTAATCC CAGCTACTCA GGAGGCTGAA GCAGGAGAAT CACTTGAACC CGGGAGGCAG 900
AGGTTGCAGT GAGCAGAGCC TGTGCTACTG CACTCCAGCT GGGTGACAGA GTAAGGCTCT 960
GTCTCAAAAA AAAAAAAAAA GGTTTCCCAG AGCCCATCTA GTAGGGCCAC ACGGTGATGG 1020
CATCTGTCTC TTGGCTCCTG TGTGGTCACC GGCCATGCCC TTCCCTGACC TCAGCTGCTA 1080
GCCCTCAGCA CATGTGACTG TGACGTCGTG TGGCAGCTGC TGAGTCCTGA GATGTTTTTA 1140
ATGGCTGTTT 1150
|
