| Tag | Content |
|---|
EnhancerAtlas ID | HS118-12461 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr3:14377430-14379060 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX1 | MA0509.2 | chr3:14377756-14377772 | GGTTACCATGGTAACA | + | 7.52 | | RFX1 | MA0509.2 | chr3:14377756-14377772 | GGTTACCATGGTAACA | - | 7.5 | | RFX2 | MA0600.2 | chr3:14377756-14377772 | GGTTACCATGGTAACA | - | 7.58 | | RFX2 | MA0600.2 | chr3:14377756-14377772 | GGTTACCATGGTAACA | + | 7.66 | | RFX5 | MA0510.2 | chr3:14377756-14377772 | GGTTACCATGGTAACA | - | 7.75 | | RFX5 | MA0510.2 | chr3:14377756-14377772 | GGTTACCATGGTAACA | + | 7.7 |
|
| | 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 |
| GH03I014332 | chr3 | 14374089 | 14378190 |
|
Enhancer Sequence | CCCACTGAGC ACTGTGCATG CCTGGCCTGG CCAGTCCTCG GGGCAGCACT GAGCAGCCAA 60
GATTGTCACC GTCCCTGTTT ACAGACAAGA AATAGAAGGC TACTACCCAG GAACGTGTCC 120
ACCTTTGCAC AGCTGTGCAG CTGTCCAGGG TCAAGTTCGG GCACAGGTTG TCAATCTCCA 180
AATGCAAGTT ATTTTTACCA CGGCTAGATT AATTACCCAC CTGTCTTTTA CCTGAGGGAA 240
CAAATGAAAC AATATATGTG CAAAGGGTCT AGTACTGTGC CTGGCACAAA GGAGTGCTGG 300
TAAGCAGTTA GGATTAGATT GACTGTGGTT ACCATGGTAA CACCAGACTT GTCCACTGTC 360
CCCAACACTG GGAACTGCAG AGTAGTGGAA ACACCTGCAA GCCAGAAGGA GGGGTGTTGA 420
GCAAGAAAGT GTGGCCTCGG CATAGAAGCA TTTACATTTT TCTTTTTTCT TTTTAAATCT 480
TGTAACGATC AGTCACACTA GAGCCCCATC CCTAGGGCAG AAATTTTTTT CCCTTTGAGC 540
CTCAGTGCTG AGTACTGAAT TACACCCCCA TCCCCGCCAT GTGCCAGGCA CATGATCCTC 600
ATTGGCCCAG GCAAGCACCA CCCTCCATGC CAATTTCCTT ATTTACTCTT CTCTTTTCCT 660
GTTTGCCAAT GCAGGTGACG AACTTGGCCA GCACAGGTGA CCAGTCTACA GGGTGGAATG 720
CCTGCCCTTT TGCACGCATT CTTGCAAAAT GCATAAGCTT GTATTTCTCA GTAAACTTTT 780
CAAAGTAAAA CATTCATGCA GAAAAAAGCA CAAATGACGC ATGTAGAGCT TTATGCATTT 840
TCACAACCTG AGCACACCCG TGTCACCCAG AATGAGAAGC AGAATATAAC GGGCATTGTG 900
GAAGCCCCCA CATGCTCCTT CCCCCAAGGG GGTCACTCCC CTGACTCTGA CTCCAGAAAG 960
CAGAAGTAGC TGTCCTGTGC TCTATACAAA TGGCATCCTG CACCATGTAC CCCTTGGTGC 1020
TTGGCTGCTG TTGCTCAACT GCACATCTGT GAGATTCACC CAGGTGGTTG TGTCTGGTTT 1080
GCTCTGGTTC GTTCGCTCTC ATGCTGTCAC ATATTCCCTT GTAGAAAACT ACCCCAGGCC 1140
ATTTGCCCAG TCTCCTGTTG TTAGATGTGT GGGTTGTTTC CAGCTTGGCG CTATTACAAA 1200
CAGGGCTGCA CATTCTGGAA CAAGTCCTTC GGTGATCATA AGCACACGCT TCTGTTCGGT 1260
AAACGGCTAG GGGTGGTATT GCTGGGTCAC AGCATATGTG TATGTTGAGC TTTGGTAGGT 1320
TCTGCCCAAG TTTTCCAACG TGCCTATACC GTCTGATACT CCTGCCAGCT GCACGTAAGA 1380
GTTCCAGTCG CTCCACCTCT TCACCAACTT GCCATTTGTC TGTGTTTCTC CTCGCAGCCA 1440
CTGTGATGGG TGTGCCTGGT TTTGGATTGC TGTTTTAGTT CTCACTGTTG CCTCTGCATC 1500
CCTCTTGATA GCTGGAAGCA ACAGCTCCTA TGTGCTGGAC ACTTCATACA TACTAGCCTC 1560
TAGAGCTTAA TCTTACACAC ATTATCTCAC TTAATCGTCA CAGCCACCAT TTGAGGGAAG 1620
TACATTTTAC 1630
|
