| Tag | Content |
|---|
EnhancerAtlas ID | HS053-17076 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr17:48575010-48576200 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr17:48575878-48575893 | GAAGTTCAAAGGTCA | + | 6.45 | | NR2F1 | MA0017.2 | chr17:48575884-48575897 | CAAAGGTCACAGG | + | 6.44 | | Nr2f6 | MA0677.1 | chr17:48575879-48575893 | AAGTTCAAAGGTCA | + | 7.12 | | Rxra | MA0512.2 | chr17:48575879-48575893 | AAGTTCAAAGGTCA | + | 7.12 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 48575400 | 48575980 | | chr17 | 48575264 | 48575793 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I050497 | chr17 | 48575246 | 48576046 |
|
Enhancer Sequence | GTGGTGGTGC AGCTGTGGTC CTAGCTACTC AGGAGGCTGA AGTGGGAGGA TTGATTGAGC 60
CTGGGAAGGT CAAGATTGCA GTGAGCTATG ATCGTGCCAC TGCACTCTGG CCCGGGTGAC 120
AGAGTGAGAC CCTGTCTTAA GAAAAAAAAT AAAAAAGCAG AAGGAAGGTT CACATGATCT 180
TCTTGCACCT GCTATTTTTC AAATGCCTTT AACTCAAAAT AGTCAATAAG CCAGAGCAGC 240
AGATTTTAGG GTAGCATGTT CTTAACTCCA CGGTGCCCTG GGCATGCTGG CTCTAGAGAA 300
CACAGGTCTT GAACAGGAAT TCCTGGTGCC TGACAAGACA GAGAGAGACC TGTCATTTCC 360
CTGTGCTGCT GAAACTTCAG TAGACAGCCC TGACTCCTGG AAATTTTTCC CTCTGGCTCA 420
GCATAGAATT TGTCACCTCC TGGGTGGCTG GGAGGCTGTG CACCATGAGG CCCACTGGCA 480
GCCTCCAGGC AGTGGGCACC CACACTATGT GACTCCTCCT ACCAGTGCTC CCTGCCTTCT 540
CTCAGCAGGT CAGGCAGGAG CGGCTCCATT CCTCAAGTGG CTGACTAATC CGGGCAGGGA 600
CTGCCCCACC TGCCTCCCAG ATCCCTGACA CCCGGGACAC CCCAGAGGTT GCCTTTCCTC 660
TGCCCTCACT CTAGATTAGG CCTCTCTTGG AGCCCTCCCT GCAGGCAGGG CCTCGGCTTA 720
GGGAGGCTGC TTTAGATCTT CGGGGAAGTT GCTGAGGAAA TGTGCCCCTC CTCCCAGTCC 780
CCACCAAGCA TGGACCCTTC AGATTAATCT ACTAACAATA ATAAGATGAG CTGTAAAAAC 840
CATCAGGCTG GCAATCCTCA GCTTGAGCGA AGTTCAAAGG TCACAGGACA ATTTAAGGAT 900
CCTGCTCACA CACCCTAGTT TGAGCACAGG AGCCCTGAAT GGCTCCCACC TGGGTCCCCG 960
GAGTGTGCAT ACTGTGTTCA GATTCCAGCT CTGCTGCCCA TTCACTGCTT AATCCTGGGT 1020
GGGGCACTTA GCCCTGCTCT GCCTCAGTTT CCTCATCTGT AAAATGGGAA TGCTAATGAT 1080
ATTCTCTACC TCACATGGTT GTAAATGTTC AGGAAGTTAG CACCCATAAC TAAAACACCA 1140
AAGAAAAATA GATACATTGG AGTTCATCAA AACTTTAAAA ATGTTGTACA 1190
|
