| Tag | Content |
|---|
EnhancerAtlas ID | HS113-35636 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr8:22962470-22963940 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr8:22963776-22963797 | ACCCTTGCCTCCCCCTCCTCC | - | 6.43 |
|
| | 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 |
| GH08I023105 | chr8 | 22962816 | 22963959 |
|
Enhancer Sequence | CCTGTCAGGG TGACTTCAGA TGAGCCTGGA GCTGAGTTCA GTTCCTGACC CCAGGTCCTG 60
GCTCTGTCAA TGCTGGGCTG GTCCAATCTG TGCGCCAGGT CCTTCCACAC CATTCCTCTC 120
TCTATCAAAG TAGGAATTGA GAAGTTCCAA CGGCTCAGAA TCTCGGACTC TCAGGCTGTC 180
AAGGACTCCT GAGATTGAAG GTTGTGAATG GCTGGGCCCT GCCGTGCTCC CCCTCTGGCT 240
CTGTGACTCT GGTGTGGCCC CAGCTCCTGC CTGTAAAGTG AAGAGGAGGT AAAAATCTTC 300
AGCAGCCCTG TGTAAACCTC AGAGGGCTGT GTTACCAGGT GTGGGAGGAC AAATCACATC 360
CTCAGGGCTG GTGTCACTCA CTCTGGACTG GATCCCCAGG CACCTGTCCT CCATCCAGCA 420
GAGGCTGCCC CTGTTCCTAC CTGCACCCTG GTACTTGCTC CCTGAGCTTG GGGCAGAAGC 480
TTCTGAAGAC TAGGGTGGAG CACCACGGGG AGGGGCCATG GAGGAACAGA GGAGCCAGAC 540
GTCAAGTGAG GACAGCGATG GCACTGCAGG GCCACAGCCT GGTTTACCTG CCATGCTTCC 600
AGTTGTCCTT CTGGTAGGCG CCTGGCCCGG GTTGTAGTTT GAAGAGTGAG CAGGAAATGT 660
CTCCATCCAG GTGGCTGCAG ATGGCTACTC ACCCAGGCTG TACTGAGAGG CCACAGTCCC 720
AGTTCTGGTC CTCTGTCGTG TATCCAGGAG TGGCAGGGCA GTGAGGCTCT AGCTTCTAGG 780
TCAGGGATGG GGACAGTGGG GACAGTGCCA TGCCCCGAGC CTCTGCCGTT GGGCAGCTGG 840
TATCCTGCTT CCAGCCAGAG AATGCACATC TTCATGTAGT GGATTTCCTA ACAACCCGGG 900
GAGATGAAGG TAGGTTGTTT TTCCTGTTTT ACAAGTGGTA AAATGAGATT CAGGGCTAGA 960
GTTCTCTGAG CAGCTGCTTC TCTGATCTCT GTCCTGCCCT TGGCCTCTGG GAGCTCTTAT 1020
GGTTCCTCAG CAGAGTTCAC AGGGCTCTTG GAGCCTGTCC TTCGGCCTTG AGCTGAGGCC 1080
ACAACTGCGC GCACTTCATA GGCTTGAGGG GAAAGTGATT CATCCAGGAA GTAAACAGTG 1140
AGCCCTTTAC TCTGAGAACA CCTGTGCCTG GAGTCCGCCG GAGTTTGGGA GGACAAATGA 1200
ACCCCATGTG AATCCTGTTC CCTGGAGCCC GCAGTGTGGT GGGAGAGGTG ACCCAGGGAT 1260
TATATAACTA ATAGGAGGTA GCATGAAGGA GGCCTGAGAT CTCACTACCC TTGCCTCCCC 1320
CTCCTCCAGA GAGGCTGTGC TGGAGAGAGG CCATGCTGTT GCAGGGCCAT AGGATGTGGT 1380
ACTGTTGGCC TGGAAGATGT GGTTTGATTA CAGTCACCAT TGAGGGTCAG GGAGGGGAGC 1440
GAAGCTCTCC TTTAGATGCC CCCCCACCCG 1470
|
