Tag | Content |
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EnhancerAtlas ID | HS091-36700 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr4:55010300-55012550 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr4:55011704-55011715 | AGTGACTCATG | + | 6.14 | IRF9 | MA0653.1 | chr4:55010645-55010660 | AGTTTCACTTTTGTT | - | 6.15 |
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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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Enhancer Sequence | AAAAAAAAAG GATACATGAA GGCCTAAGTG GATTTTGAGT TTATCTAATT TATTGTTCTC 60 TAATAGGCCT AGAATATAAA ATAAAGAAAT AGGATAATAC TTTTTTTTGT ATTGCTTCTG 120 AAGTGATACA AATGAAATTA TATCTTCCTC AGACCTTCTA CAAGCTATAA AAATTCATAG 180 ACTATTTGAA AATAAGCCTT GCTACTAGTC TTATCAAAAA CTTCAAAATG TTTCCACTTC 240 TTTGAAGTGC AATTGGTGGC ATGAAAAGAA CCCAGAACTA GAAGATGAAG GGCACAGGTG 300 GGTTTTAGCC CTGGCTTCTT TTTTTTTTTT TCTTTTTTGA GACGGAGTTT CACTTTTGTT 360 GCCTAGGCTG GAGTGCACGA TCTTGGCTCA CTGCAACCTC CACCTCCTGG GTTCAAGTGA 420 TTCTCCTGCC TCAGCCTCCT GAGTAGCTGG GATTACAGGT TCCCACCACC ACACCCAGCT 480 AATTTTTGTA TTTTTGGTAG AGACGGGGTT TCACCATGTT GGCCAGGCTG GTCTCGAACT 540 CCTGACATCA GATGATCCGC CTGTCTTGGC CTCCCAAGGT TCTGGGATTA CAGGCGTGAG 600 CCACTGCAGC CGGCCTAGCC TAGCCCTGGC TTCTTTTCTT ACAAGTTGTG TGTCCTTGGG 660 CATTTATTTA ACTTTTCTGA TCTGCAGTTT TCTTTATCTG TAAAGTCAAC AGTTGTAAAG 720 ATTAAATGAG ATAACTTTTG AACAGTGCTT TTCAAACTAG AAAACACCGC AAATATTTGA 780 TTATAAGGTA GGTTTGTCCA AGTCCCAACA GCTGTGGGAG GACTGAAAAT AAAAGATAAA 840 ATTTTTAAAC TTACAATTGT ATGTGCTAAA GGAAGATGGC CAGGATGGTG AAGTGTGCAG 900 TGACCTTGTG GTTAGAAATG TGGTTGGAGG AACTAAGACT GTTACTCTGA AGCCTGAACA 960 CTGGGGTTGC AGAGAGGAGA ATCAATATTT ACAGCCTGGC CTGGTGGGAA TCCTACTGTA 1020 TGACTTGGCC TTTAGCAGTG TCAGATTTTT AAAAATATTC CTGTTTTATT TAGAAATGAG 1080 TTATCACCTC GCCTTGCTCA TTTTCCTCTC ATCTTTACAT TCCCTTAATC CAAAAACCAG 1140 GAAGGATGCA GGCTTAGGTC TTCAGATGTC TCAGGCTGAT CTCTCTGTGC TTATAGAATC 1200 TTTTTAAGGC CACAGGAGAG GTAGGTGACA TCTGGATGTA GTCTCAAAAC AAAGCTCAAC 1260 ATGCATATCT TGGTGGAAAT CTGAAGGAAA TGGAACAGGA GGAAAATGAA GACACAACTT 1320 TGAGGCACAT ATGGATTGGA AGTTGTCTAA TGGAAGGTCT GGATACCTTT CAGAATTCTC 1380 AGAGGATATA CTTTTTAAGG TATAAGTGAC TCATGACAGG AGGAGTGGAG AGCTGGTGAC 1440 CAATTTGAAA ATTGCTCAGG AATGCGGATT GATGTTTGGA ACATCAATTT CCATAGTTTA 1500 TATACTTTCT ACTATTCAAT CAAATTAAGA TTGATGTTTG GAACTCCAAT TTCCACAGTT 1560 TCTATTGCTT CTCTTTTCTC ATAATAGTCT TTCTACCTCT TTTTATTTAA CCAAATAAGA 1620 CACAGTGAGT TTAATGAATT TTGGGTTTTT TTTCCCCCAG TTGGGAAGAT CTGTCAATAT 1680 TTCATAGGCA AGCAAAAAGA GGCACTAAAA GGGACCTATT AAAATATTTT AGTCACTTCT 1740 GAAGATCCAA AGACAGGTTC TTTTTTTGCA AAGCTTTATT CTCTTTTTAT GAATTCCTCT 1800 TTTTGCTGAT TTGTCTTTTA TTTCTTTCCT TTTTTTTTTT TCTTTTGAGA CAGAGTTTCA 1860 CTCTGTCTCC CAGGCTGGAG TGCAGTCGCA TGATCTCGGC TCACTGCAAA CTCCACTTCC 1920 CGGGTTCAAG CGGTTCTCCT GCCTCTGCTT CCTGAGTAGC TGGGACTACA GGCACACACC 1980 ACCATGCCCA GCTAACTTTT GTTTTTTTTA TAGAAATGGG ATTTCACCAT GTTGGCCAGG 2040 CTGGTCTCCA ATGCCTGACC TTAAGTAATC CACCTGCCTC GGCCTCCCAA AGCACTGGGA 2100 TTACAGGCAT GAGCCACCAT GCCCAGCCTG ATTTGTCTTT TGTGATTACT CAAAGATCAA 2160 GCAGCTCATA CTATGTACAT CAGTTTTACA GACCTGGCAA GGTAGCCCTT TGGCTTGCCT 2220 TCATAGCTGT GAACCTGCAA TTAAGTCATC 2250
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