Tag | Content |
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EnhancerAtlas ID | HS086-06282 |
Organism | Homo sapiens |
Tissue/cell | HEK293 |
Coordinate | chr19:1987690-1990000 |
Target genes | Number: 29 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxq1 | MA0040.1 | chr19:1988549-1988560 | AATAAACAATG | - | 6.02 | KLF4 | MA0039.3 | chr19:1987702-1987713 | GGAGGGTGTGG | - | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 1987691 | 1988147 | chr19 | 1988308 | 1988572 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I001988 | chr19 | 1988581 | 1988730 |
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Enhancer Sequence | CCTGCAGCAC AGGGAGGGTG TGGGGGAGGG CCGGGCTGCA CCCCAGGATC CCGAGTGCCT 60 GGGAGGACAC GCTCCTTCCC CCTAAGATGT CTGCGTCGGA CTTTCAAGGT GCAGGGACCT 120 GGGCAGCCCC TCCCCGGGGG ACTAGCCACC AGCCATGGCC CCTGCTGCCT GGGCTTTTAG 180 GGAGAGGTCC CAGGGCACAG ACCAGAGGCC GACAGATACG CTCACTCAGG GGCGATGCCT 240 CAGGGTCTGA CAGATGCACT CACTCAGGGG TGATGTCTCA GGGTCTGGCC CCACTGTAGG 300 GACCACCCGT CACTTCACTG TGGGTGGGGG CGGGGGGCTC CACTGCCTGT TCTCTCAGGG 360 CCATTGGCTG GGAGGGGTCA CTGTGGCTCC CTGCTAGGCC TGTACCCCCC AGGCTGCAGC 420 CCTGGCTTCT AGAAGCAGTC TGGGGGTTCC TCTCCACGGT GGGCCCTAGG CAGACACCTT 480 CTCAAGCGCT TACACCCCCA GGGGTGATGG CTAGCGGACC CCAGGCAGAC TCCAAGAGCC 540 AGGCTCTTAA TCCCGGTGCA GAGATGTCAC AGGCAGAGGG ACTGTGCATG GGATGTGAAG 600 GGGCTCTGGG TAGGGAGGGG AGGCCAGGAG GGGCAGAATT GGGGGTCCAC CATCCACCCC 660 CAGGAGTGCC AGGACACAGC ACCCTCTGCT CTAATGAGAG CAGCCCTGCC TGCCTGAGAC 720 CTAATCACTC ATCAACCAAG GTGGGCTCAA CTCCGCATCG CTCAGCTGCA AGCCAGCCCA 780 GTGCAGACAC AGTTTAATAA CTGGTGAGAA ACAGACCATT ATGGGTTAAG TGAATCAGGA 840 AGACTGAGTA TCAAAACTCA ATAAACAATG TTAACAATTT TTTTTTTTTT TGAGACGGAG 900 TTTCGCTCTT GTCCCCCAGG CTAGAGTGCA GGACGGAGTT TCGCTCTTGT CCCCCAGGCT 960 AGAGTGCAGT GGCGTAATCT CGGCTCACCG CAACATCCGT CTCCAGGGTT CAAGCAATTC 1020 TCCTGCCTCA GCCTCCAGCA TAGCTGGGTT TACAGGCATG CGCCACCATG CCCAGCTAAT 1080 CTTGTATTTT TAGTAGAGAC GGGGTTTCAC CCTGTTGGTC AGGCTGGTCT CAAACTCCTG 1140 ACCTCAAGTG ATTCCCCCCA TCTTGGGCCT CCCAAAGTGC TGGGATTACA GGAGTGAGTG 1200 ACCCAGCCTG GCCAACAATT GTATATATTT TTTTATTTTA AATGGAGTTT CACTCTTGTT 1260 GCCCAGGCTG GAGTGCAGTG GCGCGATCTC GGCTCATCAC AACCTCCACC TCCTGGGTTC 1320 AAGTGATTCT CCTGCCTCAG CCTCCCGGGT AGCTGGGATT ACAGGCATGA GCCACCACAC 1380 CCAGCTGATC AACAGTTGTA TTTTTAAGAA GTATGTATCT AGCCAGGCTC GGTGGCCCAT 1440 GTCCATAATC CCAGCACTTT GTGAGGCCGA GATGGGAGGA TGGCTGGAGC CCAGTTCATG 1500 ACCAGCCCAG GTGACATAGC AAGACCCTGT CCCCACAAAA AAATACAAAT ATAAGCCTTG 1560 TGTGGTGGTG GCACCTGTGA TCCCAGCTAC TCCGGAGTCT GAAGCAGGAG GATCACTTGA 1620 GCCCAGGAGG TCGAGGCTGC AGTGAGCTGT GATTGTACCA CCGCACTCAG CCTGGGCGAC 1680 AGAGACCCTC TTGCTAAATC TGGCGACCTT CAGCTAAGCA AGAGCGGGGG CCGCGTGGAC 1740 CTGGGGAAGG CCAGACGGCG AGTGTGCACC AGCCCCAGGG CTCTGTCCCA GCCCCTTCTG 1800 GAAAGTTCCA GGCCTGTTTT GCTCCAGAGC TGGATGGCGT CAGGCAGTGA GCAGCCACGA 1860 GGGCAGGAGG CATCGTTAGC GCTGCCCCTT CACGTCACCC TGGAACCCAG GCCCTGCAGC 1920 AGGGGACCCC AAGGCCCACT CGGGCGCATG ACAGCCACCC CGGCCATGTC AGAGCCCTCC 1980 TGAGCTCGTC ACAGACACTG GTACCTGCAC CAGCAGGTAG CACAAGGGCG CGAGACGGGG 2040 ACTCCCTTCC CTCCTGGGAA GATGCCACCA AAACAGCTGG ACAGACACGA GAGGCGGGGT 2100 CTGGCAGTGT GCACGGTGGG GACAGAGCCG GGCCGGGGCT AACAGATGGC CCTGTGGACG 2160 CGTCCTCACA AGCCAGGTTT CTTCCTATCT GTATATGCCA GGCATCTGCC AGGCTTTCCG 2220 CAGTGAACTC GGGGGCACTA TCCTCGGTAC CCAGATGCCC ACCTGTGTGC CACTCCCCTC 2280 CCAAACCAGC CCCTGAGCCC GAGCTCTGTT 2310
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