Tag | Content |
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EnhancerAtlas ID | HS060-18256 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr19:49734500-49735640 |
Target genes | Number: 23 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr19:49734642-49734652 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr19:49734642-49734652 | GGCACGTGCC | - | 6.02 | NFKB1 | MA0105.4 | chr19:49735333-49735346 | AGGGGATTCCCCC | - | 6.78 | NFKB1 | MA0105.4 | chr19:49735333-49735346 | AGGGGATTCCCCC | + | 6.92 | NKX2-5 | MA0063.2 | chr19:49735613-49735623 | CTCAAGTGGT | - | 6.02 | ZNF263 | MA0528.1 | chr19:49735224-49735245 | GGAGGATGCAGGGGGAAAGAA | + | 6 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr19 | 49734647 | 49734800 | chr19 | 49734800 | 49735200 | chr19 | 49735224 | 49735351 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I049231 | chr19 | 49734441 | 49735121 |
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Enhancer Sequence | GCCTGTTTTA GTTTTGTTGA GACAGTGTCT CGCTCTGTTG CTCAGGCTGG AGTGCAGTGG 60 CATGACCTCG GCTCACTGCA GCCTCCACCT CCCAGGCTCA AGCGATCCTC TCACCTCAGC 120 CTCCCAAGTA TCTGGGATTA CAGGCACGTG CCACCATGCC TGGCTAATTT TTGTATTTTT 180 TGGTATAGAT GGGGTTTCAC CATATTGGCC AGGCTGGTCT TGAACGCCTG ACTGCAAGTG 240 GTCCTCCTGC CTCGGCCTCC CAAAGTGCTG TGATTACAGG CGTGAGCCAC CACACCCGGC 300 GATACTTTTG TTTTGACAGG TCACTGACCT AGTTTGGTTC AGCTCAGGGC TTCTGAGCAG 360 CCTGCTGTGG GTTGTGGTTT CAGGTGAGTT CTGACTTCAA AGTCGTTACA ATGACTTTCT 420 AATCTGTCTT CCCCATGGAC CACCCACTGG CCAGACTGGA ACCCAGATGG TGTTGAATCC 480 CTTCATTGTG TCTTCAACAT CTTTGGAATG TTGTTTAGGC TCAGATCCAC ATGCATCTTA 540 GGGGCAAACA GAGAAATTCA TGAAAGCAAC TTCATTAGGT CACTTTCCCA ATCTCCTCCC 600 TCTCCGCGGT ACTTTCTGGT TTCTCTCCCC TTTGTTGGTC CTCCAGCCAG AAAGCTGGGG 660 CCTCAGCTAC CCCACTTGCC TCACACTTCC TGTGATTGAA CCTGCATCTA CAGCGAAGTG 720 GGCAGGAGGA TGCAGGGGGA AAGAAAGCAA TGGGGATGGG TGCTGTCCCC GGGGGACCAC 780 AGAGCCTTGA TCAGGGAGGA GAGAACAGAG AAAGAAACAG AAAAAGGGGA AACAGGGGAT 840 TCCCCCACCC TCTGATCATT AAAAGGCATT CATTCATTCA TTCATTCATT CATTCATTCG 900 AGATGGAGTC TCACTCTGTC GCCCAGGTTG GAGTGCAGTG GCGCGATCTC GGCTCACTGC 960 AACCCCCGCC TCCTGGGTTC AAGTGATTCT CCCACGTCAG CTTCCCAAGT AGCTGGGATG 1020 AAAGGCATCA ACCACCAGGC CTGGCTAATT TTTGTATTTT TTGGTAGAGA CGGGGTTTCA 1080 CCATGTTGGC CAGGCTGGTC TTAAACTCCT GACCTCAAGT GGTCCACCAA CCTTGGCGTC 1140
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