| Tag | Content |
|---|
EnhancerAtlas ID | HS132-00038 |
Organism | Homo sapiens |
Tissue/cell | Melanocyte |
Coordinate | chr1:26354810-26355510 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HINFP | MA0131.2 | chr1:26355357-26355369 | CAGCGTCCGCTG | + | 6.18 | | ZNF263 | MA0528.1 | chr1:26354959-26354980 | CCCTCCCTTTATCCCTCCCCT | - | 6.17 |
|
| | 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 |
| GH01I026028 | chr1 | 26355101 | 26355250 |
|
Enhancer Sequence | TGGGGCATGG CCCCGAGGCT GCCTAAGTAC TCCCAGGTCT GCTTCTTGGA GGTTCAGGCT 60
CAGAGCCAAA CAGGCTGTAA CTGAGGAGGG TCCTAGTACC CTCTGGGCCC TAGTCATGAG 120
TCCCACACTG AGCAGGCCTG TGTCCTGGTC CCTCCCTTTA TCCCTCCCCT GGCTGGGTTG 180
CAGGCAATGG TCCCCTGGGT GGACAATTGC CAGGCTGGCT CTGAGGAGGC TGGGACTCCT 240
GCCCTCCCCC ACAGGCACAC ACAGCCTGAG TGTGGCCCTG GGCTAGGGTG GTGGAGGGGG 300
TAGGTGGGAG GAACAGAGGG AGCCTGTCCT CTGGGCCAGG GGACCTCTGG GCAGCAGTTT 360
CCTGTGTGGT TCCAGGCTGG GGGCCCAGCC CACCTCATGA CAGAGGAGCC TTTCACGGGC 420
CTGGCTTTTA GCATCGGGGA GGGCTGGGCT CAGAGGCCAC GCAGGCAAGG GGTGCTGAAA 480
GTCTGCCTGT GGCCGAGTGG GGGAGGGCAG ACGTGCATGT CTAAGTCAGG CAGGGCCTCG 540
GAAACATCAG CGTCCGCTGC CTCCCATTTT ACAGATGAGG AAACTGAGGC CAGAGAAAGG 600
CAAGGGAGGT GTCTAAGGCC ACTGAGGGCA GAGGCAGAGC TAGAATGCAG GGCTCCTGCC 660
TCCTAGTCCA ACCACAGATG CGTGGCTGGT GTGATGCTTG 700
|
