| Tag | Content |
|---|
EnhancerAtlas ID | HS133-19930 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr20:60993520-60994640 |
Target genes | | Number: 21 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr20:60993751-60993771 | TGTCTGGGGGTGTCTGGGGG | - | 6.59 | | RREB1 | MA0073.1 | chr20:60994062-60994082 | GGACTGGGGGTGGTGTGGGG | - | 7.25 | | TFAP2A | MA0003.3 | chr20:60993685-60993696 | TGCCTGAGGCT | - | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCTGGGGGAG CAAGCAGAGG GGCGGGGGGT CAGGCCCAGC TGCTGCTTCA CCTTCAGTGT 60
CCCCACCACG GGGTCTGGGC AGAGCTGCAA TGTGGCACTC CTGTCCCCTG CACCCCCTGG 120
GGGAGCCCTG CCAGGTGAGC CCCTGTCTGT GCCCAGGCAC GGGGCTGCCT GAGGCTCGGT 180
GGTCTCGGCC TAGCATCTGT TGCTTCCCCT GGGGTCTCTG CCTCCGGCAT CTGTCTGGGG 240
GTGTCTGGGG GTGAGCAGGG ACCCTGGTGC CACAAGTGAC CAGCCACCTG TGAAAGGTAG 300
AGGGACCGAG GGGCCATTTT GTGTGTGTGT GTGTGTCATA GCTAGTGTTG AAATAAGATA 360
AGCTTCTGGG GCGGACCCCA CCAGACCCTC TCCTTGCCGT ATCTTGGGGA TCCAACCTGG 420
GCCTGGCTAG CCCCAGCAGC CCCACCTCTC TGGGTTGCCT AGGAGGCAGC CGGGTCCTTG 480
GACCTCCAGG TGGGTGTGGG TGCTCAGTGG AAAGACCACG GGGAGGTGCT GGCCCTGGGA 540
CTGGACTGGG GGTGGTGTGG GGGCTGCGGC CCTGTCCCTC GTGGGGGAAG TGGACAGGGG 600
TGGGGCCTGG GGCGTGTCCT AGAAGGAAGA GAAGAGTTGC AGCTCAGTGC CTTGACATGT 660
TCTGGATGGG TCCAGAGAGC CATAAGCTCC TGTTTCTGGA AGTGGCTGTC TCTGCCCTGG 720
TGAGCTCAGC AGGCCGGCCA GGGTGGGTAC TTCTTTCTGC CACGCTGGAG GCCGGCCCAC 780
GGGAGAACAA AGCATGGGCA GCATGGGGCC TGCGGGTGGC AGGTGGCCAT GAGGTGTTGG 840
TGGCAACCCT TGAAAGTGCC CCTCCCCCTC GGGGTCACAC TCTGGGAGTG GCTCGAGGAC 900
ATCCCCGCTT GAGGTCAGCA CTCGGGCCCA GGCAGGGTGT CTGCCACGTT GTAGCTCTGG 960
GCCTTGGGTC AGGACTCCCC TGCCTGGGCC AAAAAGACGG GGTCCATTCC CTGACTTGGT 1020
GGGAATTGGA GGTGATCATG GGTGCACAGT GGCCTGCTCC GACCCTTAGG TGAGGGCTGT 1080
GGAGACCCCT CCCTAGCCTG GCATCTGTCC CTGGCCCCTC 1120
|
