Tag | Content |
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EnhancerAtlas ID | HS091-22847 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr19:2820120-2821820 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZBED1 | MA0749.1 | chr19:2820219-2820232 | CCTGTCGCGATAG | - | 6.41 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCGTAAGTGC CGCCGCCTCC CGCGCCGCGA CCTCCGTGCC GGGCCTGCCG GGGCTCTGGT 60 GGGGCTGGGT CTGGCGGGGC CGGGTGGCCG GGGCATGACC CTGTCGCGAT AGGGTCCCCA 120 CGGGAGGGTC GGGAGCCGGC AGCTCGCCCA GGGCCCCAAC GCCCAGGATG GCACGGTCTG 180 CCCTTGCCCT GTGAAAACGC CCCTGGGTGA GAGACGCATA AGCTTTCCGA GGCCCAGCCT 240 GCAAGGAGAG GGAGAAGACG CATTGACTCT ACCCTAAAGG CAGAGAGGGG CTGCCACGCT 300 CGCACTGCAG TGAGGCCACA TCAGAGGGTC TGAGCGAGGG GCGGTCCTGC CCTCCAGGGG 360 ACACCGGGCG ATGTCTGGGG ACGTCTGTGG TTGTCATAAC TGGGGGCAGT TCCTGGCATG 420 GAGTAGGTGG AGGCCAGGGA TGCAACTCAG CACCCTGCCC AGCCCAGAGA ATGACCCAGG 480 CTCCAGTGTC CACAGCGCCC TGAGGGAGAG ACCTCACTTA TACGTTAGCA CCGCTGTCCT 540 GGTGATAAGA CAGCAAGGGT CCTTTTTTTT TTTTTTTTGA GACGGAGTCT GGAGTGCAAT 600 GGCATGATCT CGGCTCACTG CAACCTCCGC CTCCCGGGTT CAAGCCATTG TCCTGCCTCA 660 GCCTCCCAAG TAGCTGGGAT TACAGGCGTA TGCCACCACG CCCGGCTAAT TTTTGCATTT 720 TTAGTAGAGA CGGGGTTTCA CCATGTTGGC CAGGCTGGTC TCGAACTCCC ACCTCAGGTG 780 ATCCACCCGC CTCAGCCTCC CAAAGTGCTG GGATTACAGG CGTGAGCCAC CGCGCAGCTG 840 CAAGGGTCTA TTCTGTTTAT ACCCACCACC CATGTTGAGG AATGAGGGAG GCAGCTGACC 900 TTTCTGCTGC TCTAGCAACC CCAACCTCCC TGAACTCTCC CCTACCCAAA CAGGTTGGTT 960 TCTTTTTCTT CTTCTTTTTT TTTTCTTGAG ACAGTCTCGC CCTATTGCCC AGGCTGGAGT 1020 GCAGTTGCAC GATCTCGGCT CACTGCATCC ACCTCGTGGG TTCAAGTGAT TCTCCTGCCT 1080 CAGCCTCCCA AGTAGCTGGG ATTACAGGTG CACGCCACCC CGCCTGGCTA ATTTTTATAT 1140 TTTTAGTAGA TACAGAGTTT CTCCATGTTG GCCAGCCAGG CTGGTATCGA ACTCCTGACC 1200 TCAGGTGATC CACCTACCTC GGCCTCCCAA AGTGACCACT GCGCCCGGCG CCTTTGGTTC 1260 TTACATGAGC CTCCTGGAGC TGCTGTGACA ATGCACCACA AACCAGGGGG CAGGGGGAGG 1320 CTTGAAATTT ATTCTCTCAC AAGTCTGGAG GCCAGAAGCC CAACATGAAG ATGTGGTGGG 1380 GCCGTGGTGC TTCTGAAGGC TCTGGCGGGA GGATCTTCTC TGTCTCTTCC AGCTTCTGGG 1440 GGTGGCCTGC CATAGTTGGT GTCCCTTGGC TTGGGGCCAC ATCACTCCAA GCTCTGCCTG 1500 CATCATCATG TGGCCTTCTT CCCTGTGTCT CTTTCTCCTT TTTTGTTTTT ATTTTTATTT 1560 TTTGAGATGG GGTCTCGGTC TGTCACCTGG CTGGAGTGCA GTGGCACGAT CTCGGCTCAC 1620 TGCAATCTCT ACCCCACAGG ATCAAGCAAT TCTGCCTCAG CCTCTCGAGT AGCTGGGATT 1680 ACAGGTGCAC GCCACCACAC 1700
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