| Tag | Content |
|---|
EnhancerAtlas ID | HS133-13380 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr17:74410450-74411760 |
Target genes | | Number: 34 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Sox3 | MA0514.1 | chr17:74411494-74411504 | CCTTTGTTTT | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65659 | chr17:74410140-74411765 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 74410505 | 74410883 | | chr17 | 74410960 | 74411663 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I076414 | chr17 | 74410478 | 74410930 |
|
Enhancer Sequence | TGAGATGAGG GAGGTAAGAT GAAATTACAC CTGAAAACAG TTATACACAA GTAAATAGAG 60
CACTAAGCTG GGTGGGGAGA CCAGAAACTG AGTCCTGTCT GGATGGCGGT GGGGGAAGGC 120
AGGAGGACCG GGGTTGCAGG GGAACTGCAC ACCAGGGACA GCCCCCACGC CCTCACCCCT 180
GACACCCTCT CTGATCTCAC AACGCAGACT CTCAGGCTGG GCAATACAGT GCTGCTGCAT 240
CACCGCCTGG AAACTCGGCT GCAGCTCGCC AGCTTGCTGG AATGGCCTGG AGGCACAGCC 300
TGCCCGAGGG ACAGAGAAAG GGGACTGAGT CCAACTGCCT GCTAAGTGAG GGGGAAGGAC 360
TGCAGAGCTT GGCCTGGCAG GGGGCCAGCG GGCTGGTCTC TGCAGATGCT GCGGTGTTTG 420
ATAAGCAATA TGTGCACTTG GCGGCAGGAG CTGGGAGCCG AGGAGCCCAG CCCTGCACCC 480
CTCTGTCTTG GCTCTGGGCT TGTCAACCTG GCTTAAAAAA AGACAAGAAC AGCCCAGGCC 540
TGGCTCCTGC ATTTGAAGGG AGGGGACAGA TGGGCATCTT TAGGAGAAGG CCGCCTCCTT 600
CCTCAAAAGT ATAAGTAGAA GGCAGAAAAG TGATCAGCAT GATTCCATGT TCTGTTCTTG 660
TCAGGCCTGA CTGGGTATCA CTACCTAACC AGTGGCCCCG GACTGCTCCA TTTCAGATGC 720
GACAGGCTGC GGTCCTGTGG CTGCCGGGCA TCCCTGAGAA CAAGAAGGGA GTCGGCCAGC 780
TGGCCAGGCA CAGAGCAAGT TCACAGCCTC AACACCCCTC AGTGTCTGAT GCCATGTTAG 840
TTCACGGAAT GAGGACCCAG GCTGCTAATC ACACAAACTG ATCCTGACGG AGCCTGCCAG 900
GAAAGAACCC CACGTGCACT GCCTCTCCCA ACCCTATGAC CCCCACGAAG GAGGCACCAC 960
TCTTGTTCTC ATTCCACAGG AGACTGGGTG GCTTGGAGAA GTAAGTGAGC TGCCTAAGGT 1020
CACCCAAGTG CCAGGACTCC AGAGCCTTTG TTTTGCTCAC CTGCCCTTCC TCATTTGACC 1080
TGTCTGGTCT CCAAGCATGG CCCTTGCTAC ACCTGGACCA ATTGGAACCA TGCTGCCATT 1140
CAAGTGTGGC CCTGGGCCTG GCGAGGTGGC TCACACCTGT AATCCCAGCA CTTTGAGAGG 1200
GCAAGGCGGT TGGATCACTT GAGGTCAGGA GTTGCAGACC AGCCTGGCCA ACATGGTGAA 1260
ACCTGGTCTC TACTAAAAAT ACAAAAATCA GCTGGGTGTG GTGGTGCGCA 1310
|
