Tag | Content |
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EnhancerAtlas ID | HS091-11470 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr13:25179720-25182080 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
YY1 | MA0095.2 | chr13:25181802-25181814 | TCAGCCATCTTG | - | 6.04 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTTCTTAAAA TGGCTATTTC TTCTTTCCGC TCTTGGATCC CTTTATCTTT ATCTAGGACC 60 ACTAATCTTT GGATTAGTTT TCAATTTTCT TCTGAATCTT GATGAGCTTC CTTGCCACCC 120 AGATTCTGTA TTCTACGTCT GTCATTTCAG TCATTTCCAA CTGGTTAAGA ACCATTGCTA 180 GGGAGCTAGT GGACTCATTT GGAGGTAAGG GGACACTGGC TCTTTGAATT GCCAGAGTTA 240 TTGTGCCAAT TCTTTCTCAT CTGAGAGAGT TGGTATTCCT TTAACTGTGG CGTAAGTTGA 300 GTATAGTCAG TTGGCTGCAT TTTTCTGAGG GCCAAGGTTC TGTGCACGGT CTTTATTTGT 360 GGCTGAATTC TCACCTTGGT TTTATAGGAA GGTATATTAG CAAACTATTT TTGTAATTTA 420 GGTTGACTTC CAGTAGATGG CACATAAGAG TAATGGTTGG TAGATAGAGC TTAGCCACAT 480 GGCTCCTTTG TATTTCCTGG TGTTTCCGGC TGTGCTCTGC AGTACAGTGG GAAGAGAGGT 540 GACCACCTCG TCAGGTCCGC TCCTGGGCAC TGGGGAAGCC CCTTCCAACC AATGGCACTG 600 TGCCCATGTT TCTTTTGGCA GGTGCGCTCT CTCACACAGA GGCTGTGGTA GGGAGATAGG 660 CCACCCCTTT CCCAGTCAGC TGGCCCTGCA GAGGGAGACA TGCCCACTGC TGTGGTAGCC 720 CACAGGTTCA TGTAACTCAG CCCTCTCAGT ACGCTGAGAG TGTGGGCTCC TCTCCTGCTC 780 TAATGTGTGC TACAGATCTC GCCTTGGCAC TCCCAGGCTT CAACACTGCA GCCCCAGGGA 840 AAGCTCAGGC TTTTTGTTCC CTCCTCAGCT TAGGGACAGC AGGGATAGGG ACCCCGGCAG 900 TGGTAATGAC AGGGGGCCTA TCAGTTGCCT CTGGGGACTC TATCCCAGAC AAATGCAAAA 960 CCACAGCCAA TTGGGGTGAT CAGCCAGGGT TGGGGCAGCT GTGCTGCTGG GCCCAAGCTG 1020 GGGGCCCTGC CTGAAGAGCA GGAAGGTCAG GCAACCCAAC CCTGAAGATA GCCTGGCCTC 1080 CTCTCTGTAG GATGCTGTGA GAAAGTAATC AGGCTCTTTG TTCCCTCCCT AGCCTGGGGG 1140 AAGCAAGGGC GGGTACTGTG GTGGCAGCAA TGGCAGAGGC CTGTCAGTTG TCTTTGGGAG 1200 CTCCATCCCA GAGAAACACA GAGCCATCAC CAACTGAAGT GATCAGGCAG GAGTAGTGCT 1260 GGGGGCCCAA GCCAGGAGGC ACCCTGCGCA GTGAGGAGCA GCAGGGCCAG GGACCCATGT 1320 GGAAAACTGT CTGGCTGCCT TTCCATATGG CAGCTGTGGC ATGCTGGAGG CCCATGACAG 1380 CTGTCGGGGC TTTTTACTCC CTCTCCAGCC TGAGGGCAGT AGGGGCACAG GCTGCAGCAG 1440 TGCAGAGGGC CTGTTGGTTA CCTCTGGGAG CTCCATCCCA GAGCAATGAG GGCTGTGACC 1500 AGCCGGAGTG CTCAGGTCGG GGGTGGATGG CTGCGATGGA GGCCCAGGCC AGTGGGCCTT 1560 GCCTGGCAAG GTGCAGTGGA GGCAAGGCCT GCAGTCTGTC TGCTCCCCAG CATCATGGAT 1620 ATGGCCCCTA TCCTAGGGGC ACATGACAGA GCCTGGCCTA CCTTGTTGGC CGGGCTGTGG 1680 CAGCTGGTGC TGGGGTGCTC AGAGATCCAC ATTGGCTTGA GCAGTGGCTC TGCCCAGACT 1740 CCAAGCAGCT CTTCATGTCA GTCTAGAGCC CCAGGGTGTG TGTGTGGGGC GGGTGGAGTC 1800 ATGGAGGGTC TCCTGCGCCT GGGAATTACA AACGTCCATG GCAGAAGTAT GGGTCCCCAG 1860 GAGCTTTCAC TCACTCATCC TTTCCCTGCT GTAGGGAGCT TCCCCTTGCT CTGCACCCAG 1920 GTGGGCAACT GTCCTGCCTT ACTCCCCTCT GCTCTCAGTT AGTCACCACT GCTTCCTTGA 1980 TGAATCCCAA CACAGCCTGC TGGACGATCA ACCTGAAGAG CTCATGTTCA CTCACCACTC 2040 TCATCTCCTC TTGTGAGAGC TGCACACACT AGCTGCTTCT AGTCAGCCAT CTTGGCGCTT 2100 CAGATACTAG TTTTCTTAAG TAGAATTTAC TAACTTGGAA TAGAATCATC CAAAACTTAA 2160 GAGCAGAGAG TTTAACTATT TTTAAAAACA GAAGGATAGA AAGAGATGGA GGGAGAAAGT 2220 AATTCTAGTG GGCCGAGTTC CATAACTGCA GTGCATAGAA ATGTTTTTGT CACCAGGCGC 2280 GGTGGCTCAC ACCTGTGATC ACAGCACTTT GGGAGGCTGA GGTGGGCAGA TCATGAGGTC 2340 AGGAGATCGA GACCATCCAG 2360
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