| Tag | Content |
|---|
EnhancerAtlas ID | HS132-00632 |
Organism | Homo sapiens |
Tissue/cell | Melanocyte |
Coordinate | chr18:77217870-77219060 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr18:77218692-77218710 | GCTGCCTTCCTTCCTGCC | - | 7.34 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_11551 | chr18:77215863-77229495 | CD20 | | SE_58360 | chr18:77195352-77289402 | Ly1 | | SE_61778 | chr18:77193611-77227418 | Toledo |
|
| | 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 |
| GH18I079457 | chr18 | 77217644 | 77222092 |
|
Enhancer Sequence | GGTGTGGGTC AGGGCGTAGG GTCCTCAGGT CCCCTCGTTG GCACAGGTCG GGACGTGGGG 60
TCTTTCTGTG GCTGAGGGAA GCCCACCGTG TGGCTGCCCA CACCTGTCTG TCGATGGCAC 120
TAGGCCACGT CCACCCTGTG GAGATGATCG TGGAAAAGCC GCCATGAACC TCAGTGCGTG 180
AGTCCTGTGT GGACGCCTGC CTGTCTCCTG AGCACATGCC TCGGTGTGAA AGGGCTGTGG 240
GTCACAGGGT GGCTCCGTGT GAGGCCCTGC AGGCAGATGT GCAGCAGGGC TGGGTGGCTG 300
TTTCCCCTCC AGAATCTCCT CTGGGAGCCA GGCTGGGACA GACTCCTGGG GGAGAGCCGG 360
GGATGGATGA GACGCCCCAG GGACGCTCGC TTCTGGGCAT GAGGATGCTG TGGGGTGCAC 420
GGCACGAGGA CGCCGCGGGG AGCAGGGCAC GAGGATGCTT TGGGGAGCAG GGCAGGAGAC 480
GCCGTGGGGA GCAGGGCTCG AGGGCACCGT GGGACCCAGG GACGCTGCTG CTTCCACCAG 540
CGGCCCTCGT GGCTTTCTTT GTGGAAACAG TGGCTCAGCA TCAGCACCGG CGTGGGGGTG 600
GCCCGGCTCC GGGCGGCGGG TCCTGGCCGG TCTGGGAGGC TCCTGGGCCC GCAGGCCTGC 660
CTGTGTGGAA ACCTCGCGGG TGTGGCAGGG AAGCCTCCCG ATGACTCAGA CTGCAGGGAA 720
TTCCCTAATG ATCTGGAATA TTTTTACTCC TGCACTCGGG CAGTTTCCTA CTAAGGACTC 780
GGAGCTCTGA TAAGGCTGAA CACAAAGGCC CTTTCAGGAC CGGCTGCCTT CCTTCCTGCC 840
AGGGGCTGAG TTTTGAACAG CACGGGGGCC GGCGCTGCCC GTCCGGGCCT CCACGGAGCT 900
GGGAGCCGCC ATGGCGATGC TCTTGCCGGC GGGACGCGGC CCTGCGTCTC CTTTCCTGAG 960
ATGCGAGGTT ATTTCCATCT TTCAGCAGTC TCGGCGCTTT GTCTTGTTCT GGAAGCAATT 1020
GCTAGATAGA CATTTCTGGC CGTGAATACT ATTGCTTTTG AAAGACAATT ACTTTATGAT 1080
CCTTAAGCAG AAACAGAAAG CCTGCCCTCA CCCTCACCCT GGTCGACCTG AAACGGCCAC 1140
AGACGTCGGA CACCACGGGG AGAGGCCCCA CCTCCAAGAG GGAAGGCCAC 1190
|
