| Tag | Content |
|---|
EnhancerAtlas ID | HS052-05827 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr10:126076990-126078480 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr10:126077886-126077896 | GCCCCGCCCC | + | 6.02 | | SP1 | MA0079.4 | chr10:126077871-126077886 | CTGGCCCCGCCCACG | + | 6.01 | | Zfx | MA0146.2 | chr10:126077831-126077845 | CAGGCCTCGGCGGA | - | 6.14 |
|
| | 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 |
| GH10I124388 | chr10 | 126077093 | 126078369 |
|
Enhancer Sequence | GGTAAAAATT ATATTAAATA AATGTGTATG TTATTCTCTT GTTATATGAG TCCCAGGCAG 60
GAACCTAGGA CGGTGAGGAA AAGCTCTTTC TCCTCCTATG GCATCCACAC ACCCAGGGCC 120
TGCCACTCCT GCCCAGCCCA GGACCGTCAC TATCTCAGTG ACCAGTGGAC AGGGCTCAGC 180
AGGGCCACAC GGATCAAGGT GGGCCCCAGC CAGGCAGAGA CCAGGCCCCG CATCCTCCCA 240
CCCCCTGCAC AACTTCGGTC CCCCAATCAC CAGGGCAGGT ATGAGTAAGG CCATTGCACA 300
GTGGCAAAAA CTGAGGCCCG CAAGGGCCCA AGGACCACCA CTCAGATCCC TCCGGGCACA 360
GCCCAGCCAG GAGCTCCGGG CAGAGTCCCG GGAGGCCCTG CCCACAGGGT CAGAGCGCCC 420
CTGCCCCCGG CCCAACGGAT GCGCCTGTCC AGGATCACCA CCTGTCAAGC TCGCTGCAGC 480
GCGGGAGGTG GGGTGGACCC TTCCCTGCCC CGGAGCCCAC ACCTCTGCAC GGTGAACCGA 540
GGCGCTCCGA CGGGTGCGCG GACAGCACCT GGCACTGAGG AGGTGAACGT GACTCCCACA 600
CACGCGGGAC TGAACCAGCG CCCCAGAGTC CCCAGAACAC GCATGGGCCC GCGGGGCCGC 660
AGCCCACGCC CGGGACAGCC GCCCGCAGTC TACGCAGGGA GGGGCCGCGG GGCTCTGGTT 720
TCTGCAAGTT CTGAATTGTC TCCAAGGAGC ATATTCCAAC GTCAGAATAA TAAACTTTTA 780
CAGAACTGTA TTGCTCTGCA GCGCGCGGGG GGACTCGGCC CAGCGAAGAG CGAGCGCCCT 840
ACAGGCCTCG GCGGAGGAGG GCACGGTCCC CAGCGCGGCT CCTGGCCCCG CCCACGGCCC 900
CGCCCCAGCT CCCGAGCCCC GGCCTCGCGC ACGCGCATCT CGCGGGCTCG CAGGACGGCC 960
GGGAAGCAAC GCTTTGCGGG CAGCGCCCCC TGCCGTCCCA ACGCGCGTGG GGCCCTATGG 1020
CTGCGAGCAG TTCCGGCCAA AAGCCCCAGG ACCCGGACTT GGGGTTATTG ACTTGCGCGT 1080
GGGCGCTGAG TCTTGGAGGG GAGGGGACAA CTCGCCACAC CCCCGTCCTC TCCCTGGAGC 1140
TCGAAGCCCC TTTCTGCTGA AATGGGGCCT CCTTTTCTCG GGAAACTGAC TTTGGGGGAA 1200
ACTAAGTCTC AAGGGGATCT TAAAACCCAA GACGGGGGAA TGGGAACCTC ACAGGACGTG 1260
GGGGCGCTTT TCTGGCCATC TCTATATAAA ACCTGCCGGG GGCCTCAGAC CCTGGCTCCT 1320
CTGTCAGTTC CCAAGACCCG TCGCGCGCCC ACCTGAGCCC GGTGCCCACT GGATGGGGGC 1380
TCAGGCTCAC CTGGTCAGTC CTCACCCCCA CCTCCAGAGA CCAGGCAGTC ATGCCCTTCT 1440
AATATGGCGG AGGTCCCAAA AGATTATACC ATATTTTTAC TGTGCCTTTT 1490
|
