| Tag | Content |
|---|
EnhancerAtlas ID | HS133-00059 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:2019160-2020290 |
Target genes | | Number: 24 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SOX10 | MA0442.2 | chr1:2019451-2019462 | GTCTTTGTTTT | - | 6.14 |
|
| | 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 |
| GH01I002088 | chr1 | 2019601 | 2020737 |
|
Enhancer Sequence | TGACCTTTTG GTGGGGGTGG CGGGGGAGGT TAAAACCTTC CTGCTCCCCT AACCGGGTAC 60
CCACTAACAG AAAATGCCCG ACTCTGGAAA GGAGTCCCCG GAGGCCCCTG AGGAGGACCA 120
GCGTCTGGCC TGTCCGGGCA CCGGGGGCAG CATCCAGGCC CTCGGGAGCC AGGCAGGTCA 180
CTGCCTGCAC CCGGGGAGGC CTGGCTTCGA GGCTGGGAAC GCTGGGACGG CGTGAGGGAC 240
AGGCTGCTGG TGCCTGGCGC GTGCTGGCCG CCTGGACACT CAGTGAAGAC GGTCTTTGTT 300
TTGATGGCGG CAGAGCCCAT CCTGAATAGC GGCTTTCTCT GCTGTGTGGG TGGGGGCCTC 360
GGGCTCGGAT GCTGCCTGAG TTGGGGTTTT GGTTTTACAG TTTCCCACTC GTGTAACTTT 420
AAGGAGGCCA CTCAGCAGTG TCCTCACCTA CCTGGCCCAG ACTCCGCCTC CCTCATCTGG 480
ATAACGCCCA GCACACCTGA GAAGAGGCAC AGCTCTGCCC CCGTCTGTCC CTCGTCCTCC 540
TCACTGCTCC CTCCCCCTTG CCTGGATGGT GCGCCCCATG GGGTCTGCAC GCCCCTCCCT 600
CCGCCTCCCT GTTCCTCCCC TGCAGTCTCA GCTCGGAGGC TGCCCCTTTC CATCGTGGGC 660
TTCCTGGGAA CCAAATCCCT CAGCTTTGGC CCTGGTTGCA TCCTTAGGGC TGAAAATGGT 720
GCCTGGGACC CAGCAGGGCT CCCTGGACAT TTGCTGAACG TCCTCGAGTC CTTGAGTGAA 780
GACGGCTGTG GCGAGTGATT GCCGCGTGAC TCAGCCTCTC CATCCCACGC CCAGAGCGGC 840
TTCCGGAGGT CCCAGAGCCC GGGCTCCAGG ATGAGCCCAG CAGAGTCTTC CCGTAGACAC 900
CATCATCCTG TGTGGAATGT CACCTCTCCT TTCTAGGTCA GGCTGTGGGA GCTTCGGAGC 960
CTGACCAAAC CCAGGTCATG TGTGCACAGC TCAGCTGCCT GGAGGCCCCT CCCAGGCGGC 1020
GGCGTCTCTT CACTCACAGA CTCCAGCTGG GGCTCAGCGC AACATAGCAA GACCCCATCT 1080
GAAAAAAACA CAAATCAGTG TTTCTGGTTG TGAAAGCAAC ACATGTTCAC 1130
|
