| Tag | Content |
|---|
EnhancerAtlas ID | HS091-22989 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:5577380-5578880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr19:5578405-5578424 | GGGCGCCACCTAGTGGGCA | - | 7.19 | | ZNF263 | MA0528.1 | chr19:5578619-5578640 | TTTTCTCCCCTTCCCTCCCCC | - | 6.99 | | Zfx | MA0146.2 | chr19:5577501-5577515 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | 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 |
| GH19I005577 | chr19 | 5577501 | 5578665 |
|
Enhancer Sequence | CAGAGTGCTG GGATTATAGG CGTGAGCCAC CGCGCCCGGC CCTAATTTTT TGTATTTTTA 60
GTAGAGACGG GGTTTCACCG TATTAGCCAG GATGATCTCG ATCTCCTGAC CTTGTGATCC 120
GCCCGCCTCG GCCTCCCAAA GTGCTGGGAT TACAGGCATG AGCCACCGCG CCCGGCCGAA 180
TATCAGGCCC ATTTTACAGA TGAGGAAACT GAATGCATAG CATGAAGGCA GTACCCGAGC 240
CAAGGCCTGG CACATAGTAG GTGCTTAGTT TGAGCAGGAT CTAAATCTCG TTTGGTCAGA 300
CCCACAGACA CACAGCTCCA TGAACAGTCG CTCCTGTCTC TCCAGGGGAC CCCAGGAAGC 360
ACTTCATAAA TATTTCAGTT CTTGAATTCT TTGGTGACTC TATACAGAGC CGCCAGGAAA 420
GGTGAGCAGG GGCGGGAGAG GCAGCTTTCC AAGGGGGGCG GAGACATGAG GCACACATCA 480
AGTCACTCGC CAGCCCGGAT ACACCAAAAT GTACACAGCA TGAGGAGAAG TCAGTCACAC 540
AGAGACACAG ACACACCCAA GGCAAATACA GCCATGATAT GTAGCAAGAG AAAAATGAGA 600
CACGTAGTCA CATGCGCAGA GACACATGCC CCCCAGAGCA AACACAGACA CACACGGACA 660
CACGCCCCAT GACAAACACA GATGCACACA GAGAGACACA CGGCCTTAAG CCTCACACAC 720
GGAGATTCAC CAGATCCACA CCCCAAGACA GAAGCAGGCA CGTCCACTCC TGAGACCAAT 780
ACAAACTCAC TCTAAGAGAA GCACAGACAC AACCAGGGCC TTCGCCTACC GGGGGCCGGG 840
TTGGGAGGCT CTGGAGACCC TCGACCCTTG AGGAAGCCCC CATTCCAGCC TCCACCTGCG 900
CCTCCAGGGC CTCCCACAAA GGTGGTGTTG GGCCCGTGGG GGAAACGCTG GGCGGGCAGA 960
GAGATGGGGG CTTCCGCGGC AGGAGGGGCC CAACCGGGTC GGCTGCGTTG CAGAGCGTGG 1020
CTCTTGGGCG CCACCTAGTG GGCACATGGA GTAGAGGGCC CGGCTGCCCC AAGTGCAGAT 1080
CCACATCTGT GCAGGTCCTG GGTTCATCTG TTTCTGCTTT TGTCTATTTG CGTCCCTGTG 1140
TGTGTGCGTC TGTTTCACTC TGTGTCTCAG TCTCTGTCTC TCTTCTCCCT GAATCTCTCT 1200
TTTTCTGTGT CTCGGTGTCT TTATCTCTCC ATCCCTCTTT TTTCTCCCCT TCCCTCCCCC 1260
ACGGCTTCCC CCACCTCCAG AGCCTGAGGC TTCGTCAATA AGCAAGCCAG GCATCTCCAG 1320
TGACCCAGCA CACCCCACTT ATAGCCGCAT CTCTTGGGTC CCGTCCCTCA ACGGCGTCTT 1380
GGTCCCCATG AGTGTCCACC TGCTATGACT CAGCCAGGGG CTGAGTGAGT GGGGGTGTGA 1440
TACCCAACGG ACTCTCACTC TGTCGCCCAG GCTGGAGTGC AGTGGTGCAA CATCAGCTCA 1500
|
