Tag | Content |
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EnhancerAtlas ID | HS118-09389 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr19:45786790-45788090 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAFK | MA0496.2 | chr19:45787059-45787078 | AATTGCTGAGTCATCTGGT | - | 6.01 | MAFK | MA0496.2 | chr19:45787059-45787078 | AATTGCTGAGTCATCTGGT | + | 6.51 | NFE2L1 | MA0089.2 | chr19:45787060-45787075 | ATTGCTGAGTCATCT | - | 8.12 | Nfe2l2 | MA0150.2 | chr19:45787062-45787077 | TGCTGAGTCATCTGG | - | 6.48 | Zfx | MA0146.2 | chr19:45787509-45787523 | CCCGCCTCGGCCTC | + | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I045283 | chr19 | 45786461 | 45787658 |
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Enhancer Sequence | GATGTGTGGC CTTCAGTGAC TGGCTTCTTT CATTTAGCAG AAAGTTTTCA AGGTTCATCC 60 ATGATATGGG TATCAGCACT TCATTCCTTT TCATTGGCAA GTAATATTCC ATTGCATAGA 120 TAGACCACAT TTTGTTTATC CATTCATGAA CACGTGGATT GCCTCCACTT TTTGGCTGTT 180 GTGAATGATG CTGCTGTGAA CATTTGTATC CGTGTTTTTG TGTGGCTGTG TTTTGCCGTC 240 ATTTCTCTTG GGTACGTATC TGGGAGTGGA ATTGCTGAGT CATCTGGTAA CTGTGTGTTT 300 AATAATAGTT TGAGGAACTT TCAGGGTGTT TTCCAACTCT GTTCGTTTTA CAGCCCTGCT 360 TGTCTGCAGG GGTGAAGTTC TTACTCTGGG ACAGGTACTA GGCTGTCTGC TTGTCTAATC 420 TTTTTTTTCT CTGTCTTACA TATCTCACCT TATCTTTTTC TAGATCTCTC AGCTCCTAGA 480 TTTCTTCTTT TTTTTCTTTT TTTGAGACAG AGTCTCACTC TGTCGCCCAG GCTGGAGTAC 540 AGTGGTGCGA TGGTGGCTCA CTGAAACCTC AGTCTCCCAG GTTCAACTGA TTCTCCTGCC 600 TCAGGCCCCC GAGCTGGAAT TACAAGCCAC CTTGCCCAGC TAATTTTGTA TTTTTAGTAG 660 AGACAGGGTT TCACCGTGTT GGCCTGGCTG GTCTTGAATT CCTGACCTGA GGTGATCCAC 720 CCGCCTCGGC CTCCCAAAGT GCTGGGATTG CAGGCGTGAG CCACTGTGCC CAGCCACTCC 780 TAGATTTCTT TTCTTTTTTT TTTTTTTGGA GGCAAAGTCT CGCTCCGTTG CCCAAGCTGG 840 AGTGCAGTGG CGCAATCTTG GCTCACTGCA AGCTCCACCT CCCGGGTTCA TGCCATTCTC 900 CTGCCTCAGC CTCCCGAGTA GCTGGGACTA TAGGTGTCCA CCACCACGCC CAGCTAATTT 960 TTTGTATTTT TAGTAGAGAT GGGGTTTCAC TGTGTTAGCC AGGATGGTCT TGATCGCCTG 1020 ACCTCATGAT CCACCTGCTT TGGCTTTGGC TTCCCAAAGT GCTGGGATTA CAGGCATGAG 1080 CCACCGCGCC TGGCCCGCTC CTAGATTTCT TACATCTCAG TTTTAGAATC CAGCCCAGGG 1140 CTGAGTGCAG TGGCTTACGC CTGTAATCCC AGCACTTTGG GAGGCTGAAT TGGGTGGATC 1200 ACTTGAGCTC TCAAGTTCGA CACCAGCCTG GGCAACATGA TGAAACCTCA TCTCTACAGA 1260 AAAATACAAA AATTAGGCTG GGCGCAGTGG CTCTTGCCTT 1300
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