| Tag | Content |
|---|
EnhancerAtlas ID | HS132-01165 |
Organism | Homo sapiens |
Tissue/cell | Melanocyte |
Coordinate | chr5:141735860-141737190 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX1 | MA0002.2 | chr5:141736665-141736676 | AAACCACAGAG | - | 6.14 | | ZNF263 | MA0528.1 | chr5:141736724-141736745 | GCCCCCGCTTCCGCCTCCTCC | - | 6.29 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_34287 | chr5:141734813-141741679 | HCT-116 |
|
| | 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 |
| GH05I142355 | chr5 | 141735231 | 141745153 |
|
Enhancer Sequence | ATGTGACCCA TTAAAAAACT CATAGCACTT GTAGATGTGA AATAATCCTG TTCATTCATT 60
TTTGAGAATC TAAGCCCCCT GTGGGCAGGA ACCGTATCTG TGTTGTTCCT GCGGTGCGGG 120
GGCTTAGAGT AGTGACCAGC ACTTAGTAAA ACATACTCAT TAAATGACTG AATGAACGAA 180
ATCCCAGGAG GCCAGTTGAG TAGTTTTTTT TTTTTTTTTT TTTTTTCCTG GTCCCGACCA 240
TCTGATTCTC ATTACTTCTA CAGCTCGGGA AGTCTCTGCT TTGGCATTTT ATAAACCTCC 300
TGTGCGTACG TCGACATTTT AACCATAAAT CCAGAGTTTT GGGACTGCAA AACTCGAGGC 360
CAGGGGATTG GGGGAGGGGG ATAACTACCC GGAGGTCCGA AGCCCGGCGG AGCTGCCCTG 420
GGGTTGGGGG GAGGGACGGG AACCCTCGGG AGGACGCCCC TCCGCCCCCT GCCCACCCCC 480
TCGGCGGGAC ATGGCCCCGG GCCGGGACGT CCTTCAGATT GGTGCGCCGC CGCCGCGGCC 540
GTCTCCTCCC GTCGGGCGGG GTGGGGGGTG GTGAGGGACG CGATCCAGGT CGTGGCCTGG 600
CGGCGGCTCC GGCCACAGCC CCCGCATTCC GGCCGCGCGC CCCCGGAGGT GACGCCTTGA 660
GGAAGCTGTA TTTTTTTGGG GGGGAGCCGC AGGGAACCGT TGGGAGAGGG GCCCTGTGTG 720
TGTCCCTTTA AGAGCCGGAG CGCTGCCTCC GCCTCGCAGG CGCCCGGAGC CTCACAAAAG 780
AACAGGATGT TGTTGATTTG TCACCAAACC ACAGAGAGGA AATGATTGTA AATTTCCTTT 840
AAACATCCCC ACCGCGCTCC GGCCGCCCCC GCTTCCGCCT CCTCCGCCCC CGCCCGGTTC 900
GGCACAGCGG GGCCTCAGCG CTCCCGCGGG GCGCCTGCTC CCCGGCCGGG CCACGGGCCG 960
AGCGGCTCCT GGGCGCCTGC GGGAGGAGCC CCCGGCCCGG CCGCTGCCCC AGCTCGCGTT 1020
CCAGTTGCTT TTTCTACAGT TGCAGCGGAG GAAGGTCCTG GGCTTTTGTG TGAGCCCGCG 1080
CGCCGCCCTT CTCTCCGGGA GCGAATGGGA ACCGCGCGCG GGGAGCTCCG TGCTGTGTCT 1140
AGGGAGCGCC TTAGCGCGCC ATCCCCGTTT AGCCTCGCAG CTTCCCTGTA GAGGCAACAA 1200
CCGTTATCTC CTTCGTTAGG GTCTGGAGGG AAACTGAGGC CCAGGTTAGT TACGTGAGCC 1260
GAAAGTCACC AGCTCTTGGA ACGCTTTGGG GGCTCTTGGA ACACACCATG CAGGTTTAGG 1320
TCACCCCAGA 1330
|
