Tag | Content |
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EnhancerAtlas ID | HS091-13977 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr14:94501900-94503720 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
STAT3 | MA0144.2 | chr14:94501981-94501992 | CTTCTGGGAAG | + | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 94502541 | 94502599 | chr14 | 94502784 | 94503358 |
| | Number: 1 | ID | Chromosome | Start | End |
GH14I094036 | chr14 | 94502747 | 94503346 |
| Enhancer Sequence | CTGGTATTAC AAGCATGAGC CACCGTGCCT GGCCCATCCA GTTCTTTAGG ACAATGAATT 60 CATCCTCTAT TCTTAAGCTA TCTTCTGGGA AGTTGCCCTG AATCCCCCAT GTCGGGGGGA 120 GATCATGTTT GGTGCCACCA GAAAGGGCGA AACAGAATAA AGTGTAAGTT CAAGGGAGAG 180 CACAAGCCTG ACTCAGATGA GGTGGGGAGA TCAGGGAGGC TTCATGGAGG AGGTAGCTTT 240 TATTCATTTG TTTGAAAAAT ATCTCACCCC CTTCTCCGTG CCAGGCCCTG GGTGAATGGA 300 AGATGGCAGA CAGTATGACA AGCTGTCATT CCAGGCCCCC CAAAAACACC CCTGCCCAGT 360 CCCAGCTTCT CTCCTGACCT GATACTGGAC ACAGGATCAG GGCCAGATGG AAGTTTGCCA 420 TCTGTCCCAT GTGGAGACAG AAGCAACAAA AGTCATTTAG GCCTCATTAT CTAATCTCAT 480 GGCCCAGCTT TCTGCTTCTG TGGGCTGAGC TTTGGAAAAA GCTAATCATC AAAAATCCGG 540 ATGTATTTCT TCAGGTGGAG AAAGGGGTTT GTAGCATCAG AGGGCTCCTC TCTGAGCAGG 600 ATGGTATTGG GTTGAGATCA TTATCTAGTC AGTGATGAGG CTGAGAGGCT ACCAGGGAAG 660 GCCACTGTGG CCGGTGTGAC ATGAAAAAGG CCAGTTACAA CTGGGTGTCA ACAATGATGG 720 TGATAAATGA ATGGAAAACT AGATTACTAT TTACAAAAAT CCCAATTAAC AGTGACCATC 780 CACAGTGCTC TATTGCATAA AAATGGTCTC CCTGGGTTGT GTGCAGGAGC CAGCCTCATT 840 TATTTTAAGC TGTAAACTAT AAGTGGCTTT AACACCATGT CTCTCACAGT ATGTTCATGC 900 TGCAATCAAA GCGGCTCTGG GTGGGTTGGA GGCTAGAGTT GCATCTCCTG CTTGTTTGAG 960 CCCTGCTGAC AAGATAGCAC AAGGCGGAGA CCAGGCCCAC GGGGAGTTGG CTGCTAGAAC 1020 GTGTCTCCTG CAGTTTCCTT CACCCTGAAG CTTCCTTTTG CAGTTGCCTC CTCTCTGTCC 1080 GCCAATTTCT TCTCTGGCCT GGAGAGATCC TGCCTGTAGG AGGCTTGTCT TTCTGGGTTG 1140 GAATTGACCT AGACCCAGAG CTGGGCTGTA GTGTAAACTT TCGCCGGTAG GTGGTGCATG 1200 AAGATGCCCT CCTGCCCTGT GCTCCCCGAG CTCAGATCTC TGACACCTTC TCTGGCATCT 1260 CCATGTACCA GTGCCACACA CTGCGGCCTC TTCTGGTGAC CTTATCACCC CCTATCTTGA 1320 TTGTTTTTCC CTGTAGACTG TGAGCCTTGT GGGTGAGGGA GTGCTAGACG TCCTTCCTTC 1380 TGTATTTCCA GCATGTGACA CAGTGCTGGG CATGTGGATG TTCAGGAATT GTTGGATGAG 1440 TAAAAGAATG AATGAACGAA TGAATGAATG CATGAATGAG AGAAGAGGGA TGGAAGGAGA 1500 CAAAGGGCCT TATCCTCCAG CATGAAGGTT CGTTAAGTTT GAGGTACACA TTCTGTGAAA 1560 TGAATCAGGC TTCCAGTAAA AAGATGAGTT TCCTTATAAC CAGGGCTATC TCTTCACGAT 1620 GGCCCCGACC CTGACTATCC CTGTTCTGGA AATGCGGTGA TCCCAACGGG CGTCTAGGAT 1680 GCTGGTAACA TACTCCCAGC ATGAGAAGGT GGGAAGGTCT CATTCATTGT TGTCTGTAAC 1740 CGGCAGTTCA GAGGCCACCA GCTCGGGGAG TCCCGTCCGT TGCTTTTGAA ATTGTCACAG 1800 CATTTCTTCC TTCCCTATCT 1820
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