| Tag | Content |
|---|
EnhancerAtlas ID | HS053-03946 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr1:228083280-228084830 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr1:228083416-228083431 | GAAGTGCAAAGGTCA | + | 6.31 |
| | | 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 |
| GH01I227895 | chr1 | 228082987 | 228084633 |
| Enhancer Sequence | CTATAATCCC AGCACTTTGG GAGGCTGAGG CAAGAGGATC TCTTGAGGCC AGGATGGCGA 60
GACCAGGCTG GGCAACATAG CAAGACCCCA TCTCTACAAA AATGAGAATA AAAATGAGCC 120
ATCAGACACA ACTACGGAAG TGCAAAGGTC AGTCCTGGAG GCGGCGAGTT GGCAGTAGCC 180
TGAGGGTAGG ACTTGCGTCT CCCTGTGTAC CTGCCGCCTC CAAGTTCAGA TGCACTGGCC 240
GTTCTCGCTG GGGCCATGAG CCAGGCAGCA CCCGGGGCCC GGCACCCCAG GCCTGGACTC 300
CTGGGCCTCT GCTCGCTCCA GTTTCCGGCA CCTTTCCCAG GAGGGGCTCT GGGTGAGTGC 360
TGGCCCTGTA GGTCCCTCGG CCTGTCGGGA GAGCCACTCA GGACAGCGGC TTCAGGCCCC 420
CAGGCACTCT CAGCTCAGGA GGCCCGGCCT GGTTTCCTGC ATTCCAGCAG AGGGCCAGAT 480
CTGACAGGCC AGCATTCCTC TCGCAGAGCA TGCCCGGGGC GGCCACTCAG CACCAGGCCC 540
CGCTGGGAGT CTCACTGGGC AAAGGCACCC AGCATCCAGC TGCCTCCCCT GCAGGACCCC 600
AGGAGCATGG CCTGGGCTGC CAGGTGGCCT TGGAAGAGCA CAAAGAGCTG TTTGTCTTCA 660
GGCTCGGGTG AGGAGGAAGG GCCTGCCAGG AGGCTGGAGT CAGACTCTGA CTCCTTCTGA 720
CACCACGGCT CCCTCTTCCC AGCAGCTTCA GCTGGTGCCT CCCCTCTCTC AGCCTCAGCT 780
TCCCCACTGC CATCCATCCG CTCAGTCAGT TTTTCCCAGA GTGGTCACTC ATGGACTCTG 840
TTATGCGGCA GGGGCTCGAG CCTCCGCCCT GCCCGGGAGG GGCCCACAGT CAGGAGGGAA 900
CGCGGGCAGG CAGCCGTGGG TGAGGCCCAG GACAGAGGAT CCAGGGAGCT CTCAGCATCC 960
AGAGCTGCAG TCAGGGAAGG GGAGCCAGGT GAGGGGACCT CTGAGATGGG CTTTGCAGTG 1020
TGACTAAGAG TTCACAAAGA GAAGCGTGTT CCCTGCCGGA GTGTGGTCCT CAGGGGCCTG 1080
TGGTTCCAGG TTCCCATGAT TAAAGCCTGT GCCCAGGAGA GATGAGCAGG GACAGGGTGA 1140
GGGCAGATGG GCCAGGAGGC TTCCACAGGG TAGAAGCTTT GGTTACAATG CCCTTTCCTC 1200
TTCCTGCAAA GCAGTGGCCC ATGGGCCAGC CCTCCCACAC CCCCGTACCT GCCAGGCTTC 1260
GCAACAGCCC ACAGGGACAC ACAGAGCCCC TGCCCAGTAT CTCAGCTCCT GTCCCCAGGC 1320
ATCCCAGTGC ATGGAGGCTT CAAGAGGCAG AAGCCCTGTG TTTGGGAGCA GGCCTGCTGG 1380
GGACCACTAA GGGTCAGGGT CCCTCATAAG ACTTTGGGGG CAGCCTCGGA GGCCCAGGCC 1440
ACTCAAACAT GGGAGCCAGG CTGGTGGACA GGGCCACAGC CCCACCCAGA GTCCCCCAGC 1500
ACTGGGCTTG GGCCCCCGCT TCCTCCAGGG GAGACCACGT GGGTGACTGA 1550
|
| |
|
|
|
