Tag | Content |
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EnhancerAtlas ID | HS045-70178 | Organism | Homo sapiens | Tissue/cell | Fetal_lung | Coordinate | chr9:98346190-98347370 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr9:98346689-98346700 | GGGCGGGAAGC | + | 6.02 | ZNF263 | MA0528.1 | chr9:98346980-98347001 | GAGGAAGGGAGAGAGAGAGGG | + | 6.07 | ZNF263 | MA0528.1 | chr9:98346996-98347017 | GAGGGAAGAGGAGAGAGAGAA | + | 6.33 | ZNF263 | MA0528.1 | chr9:98346999-98347020 | GGAAGAGGAGAGAGAGAAAGA | + | 6.45 | ZNF263 | MA0528.1 | chr9:98347002-98347023 | AGAGGAGAGAGAGAAAGAGAG | + | 6.47 | ZNF263 | MA0528.1 | chr9:98346979-98347000 | GGAGGAAGGGAGAGAGAGAGG | + | 6.72 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTTGATATTT TTAGTAGAGA CGGAGTTTCA CCATGTTGCC CAGGCTGATC TTGAACTCCT 60 GGGCTCAAGC AATCCACCTG CCTCGGCCTC CCACAGTGCT GGGGTTACAG GCGTGAGCCA 120 CCGCACCTGG CCCACGATCT CCATTTCTAT AAAATGACAG CCACACTACC CTAGAAGTCC 180 TCTGTGGGTG TTCTGTTCCT CAACAGAAGA GAACAGCATT TCAAGAGGCA GAATCTCCTT 240 TTCAGTGCAT TCCTATCCCC CCATCTCAGT CCTGTCTCCT TCTTCCTGTC CATCTCTGGG 300 GCCCTAACCA GAAGGAGTCC ACGCTGGGTG GGAGGATGGG CGGTAGAGCA GGCTCTGTCT 360 TGGCCAGCTG CCTCTGTCCC ACTCACAGGG GGTGCAGGGT GTCCTAGGCC ACCCTGGCTT 420 TATTTACCTC CCAGCCACAG TGAGGTCTGG GAGCCACTCC CAGGCAGGGC CTTCTCCCTG 480 GCCAGCGAGT CATTTCGGGG GGCGGGAAGC AACCCAGGGC AGCGCCTTTG AGAGATGTGG 540 CTGACTCTGT CTCAGTTCTC CCGGGTGGTC AGCCTGTAAT TTCAAGATTT ACTGGCCTCA 600 CGGAGATAGC CGGCCTCAAA TGGGGCAACA CGGGTAATTA CAAGAGGCTG CTCCACTAAT 660 CCTGGGTTAC AAATGTTAGT TAGAAGGTAA ATAAGCGCCG TGCAAGCAAT TCCTGGGGCT 720 GCATGGGCCC TGTGTTCTCT TCGCTTTATT TTCTTTTCCT TAAAGAGGGG AGAAAAATGA 780 GAGGTGGTGG GAGGAAGGGA GAGAGAGAGG GAAGAGGAGA GAGAGAAAGA GAGAGACTAA 840 AAAGAGAGGC TGATTCTTAT TAATTTCATT ATGGCCACTA AGAATGAGAA AGTCTTTGAA 900 GCCCAAATTA TTTTAATACT TTTTTGGTTT GTTTTATATT TGGAACTGGA AAAAATTAGG 960 AAGCTGTATT TCTAAAGTTC AAGAGAAGTA GTGTTGCAGA TTCTGCCAGT TGGTGGCTGA 1020 ACTTGGGCTG ACAGAATGAT TTTTGGGAAA ATGTCTCCAA ACTGAGCAAA AGAAAGAAAA 1080 CTTGTGGGAC ACCTGCCCTC CTGCAAGAAG CCTGGAAGCT GGTGGGTCCT GGCTGTTGCT 1140 TTGTTGCTCT TCCCCTCCAG GCATCATCAG GAGCAGGGGT 1180
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