Tag | Content |
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EnhancerAtlas ID | HS091-35490 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr3:159720580-159722220 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr3:159721500-159721519 | TGGCGCCACCCAGTGGCCC | - | 6.17 | POU2F2 | MA0507.1 | chr3:159721853-159721866 | TGCATTTGCATAA | + | 6.29 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GCTATCTCTG AGTAGCATTC TTCCCCATGA AAAGTAAATA ATTCCACCGT GAAAGTCCAA 60 GAAAAGTAGT GTTTGGCCAG TTGTACTTCT CCAGGGGATG AGGAGCTCAC CTTTGAGCTT 120 GCATCCCAAA TTGCTAGGTG GGAGAGAATT GCATTTGTTT CTAATCTCTT GAGGCTTCAG 180 CACCCCAAGA CTAGAGAGTA GAAAACCTCA GTGGTCCTCC AGGCAAAGTG GGCCCGAGGG 240 TTCAGAACGC TCGCTCACCA TGTCTGAAAA GCATGCAGAG AGATCATAGT ACTTTGACTT 300 CTGATATAAC CTTCTGGGGT GTTTATGTAC TTATTTTTTT TGAGACGGAG CCTCGCTCTG 360 TCATCAGGCT GGAGTGTGGT GGCGTGATAT CGGCTCACTG CAACTTCTGA CTCCCTGGTT 420 CAAGCGATTC TCCTGCCTCA GCCTCCTGAG TAGCTGGGGT TACAGGCACA TGCCACCATG 480 CCCAGCTAAT TTTTGTACTT TTAGTAGAGA CGGGGTTTCA CCATGTTGGC CAGGATGGTC 540 TTGATCTCCT GACCTCGTGG TCTGCCTGCC TCGGCCTTCC AAAGTGCTGG GATTACAGGC 600 ATGAGCCACC GCGCCCGGCC AGGAATAAAA AAATCTAAAT AGAATTTTAA ATAAAACCTC 660 TCTCTGAATT ACTGAGGATT CTTAGAAAAA AAAAACACTA TATTCGTTGT AGTAACAACA 720 TATAATAATC AAAGTCTTGA ATTGATTTGA GCTCAGTTAT GACAATGTGC TACATCCATC 780 CACACACATA CAAAATTAGA AGTGCTTGAA AACCAAGACA AGGAACCCTG TGGTTTTCTG 840 GATCAACACC AGGAACGATC CCCTCCAGCC CTCCCTGGGC TCTGCTTTCT CCCTTGCCCT 900 CTTTGCTGGT TGAATATTGC TGGCGCCACC CAGTGGCCCC CATGACCCCT GCTTCAGTGC 960 CACAGAAGGC CCAGAAGGCT CAATGCTACC AGCCCTGCCT TAAGTACCAG GGTGACATGA 1020 CTGCTCCCTT ACTGAGCCAG ACCACCTGCC TGGATCTTGA CATGCATGGT CTCCTTTCAT 1080 TCTCACCACA GCCCAGGACA TAGGAGGGTC TGAACCCATT TCACAGATGG GAACAGAGAG 1140 GCTTCAAGTT AGGTTGAGAT TTTACTTACA GTCCCAAAGC TAGGGCAGCA CTGGGGCTGG 1200 GCTTCCAACC CTTCCTCTGA CTCAGCTGCA CACACCATCC TTACTAAGAG GACAGCAGCC 1260 CCTTGCTTGC TTTTGCATTT GCATAACTCT CTGAACCCAA GCTTATAAAT AACCAAGCCA 1320 CATGTTCTAT AGCTATTCCC AAAGACACAG CTTGATTCCA GACAAATAAC TAAGATATAA 1380 TTTTCTGCTC ACCTTCCAAC ACATCTTGGA CTTCAAGAGA GATGATGTCT TTCAAGCACT 1440 TACATAAATT CTGGGCTGTG GCAAGGCTCT GATCCTTTTC TTGCCACTTC TTCAGCATCC 1500 TAAACTTGCA GATGGTAACA TCTTCTGCCC TCTTCCAGAT ATCATCAGTT TTGATAACTC 1560 CAACTCCAGA TTGGCAGTGG CAGGTTTTGT TTTGTTTTGT TTTGTTTTGT TTTGTTTTGT 1620 TTGCAATGGC ACAATCTCAG 1640
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