Tag | Content |
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EnhancerAtlas ID | HS093-14751 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr19:1839340-1840670 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr19:1840260-1840278 | GGAAGGAAAGTGGGAAGG | + | 6.53 | EWSR1-FLI1 | MA0149.1 | chr19:1840256-1840274 | GGAAGGAAGGAAAGTGGG | + | 7.03 | ZNF263 | MA0528.1 | chr19:1839841-1839862 | CCCTCACCTCACTCCACCTCC | - | 6.08 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH19I001839 | chr19 | 1839780 | 1842857 |
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Enhancer Sequence | TCTGGGACTC CTGTGCTCCC CGTCAGGCAC AGAGGACTAA AAGCATCCAG GAGCCCTGCA 60 GCCTCTTCCA GGGGCTCACA GAGAAGCTGG AGTGGGCACC TCCACGGGGC GCTGCCCCTC 120 AGCCAGGGGT TCACAGGCTG TTCCTAGGAT GGGTGCCGTG GCGCCTAAGG AGGAACCCAC 180 ACACCAGGGT GACTGCAAGC ACAAGCTGTT TTTGTTACTT GGTGACCTGT GTGCAGATGC 240 TGGGGGGACG GGGTGCTGGC TGGCAATGTG GGCCGACCCC GGCCCCATCA TTCATTCCTC 300 CAGCACATGT TCTCTGAATA CCTGCCCAGG ACCTCAGAGA GGGCACGCAG CCTGCAGGGC 360 ACAAAGGGCA GGGCCCTCCC TCTCTGTCTC ATCCACTTCC CCAAAGTCCA CTTCCTCCAG 420 GCAGCCCTCC GAAGTCCTCC CTGCAGAAGC AGCAGTGCCT GGCATAGTGC CTGGGATACA 480 GAGGTGGAAG GCATGGTGGA GCCCTCACCT CACTCCACCT CCTCGGCCGT GGTGCACGGG 540 GCGGTGGCCA ACTCAGGACT GCGCAGGCCC ACTTCCATGG CTTCCAGATC CTGTCTCCCT 600 AGGGCCTGCT CCTGAGGCAG TGCTGGCTCC CTTTTGGTCT CTGAGGGCCT CTGAGCCACT 660 GTGAGAGGAG GAGGGAGGGG TCTCAGAAAA ATGGACTGTG ACCCGTGACC GTTAACAGGG 720 TGGGGATGGA CCTGTCGCCA GGACAAATGG ACAGGCTGGG AAGCCACAGG GCGGGGATAC 780 GCCTGGAGTG CACGCCAGGC CCACACCCCC AAGCACACGC TCTCTGCCAC CTTCCTGGCC 840 CTGCCCCCTG CCAGGCTCTT CTGAGCACCC CAGCGTCGAC GGAGCTGGCC CAGGGCAGGT 900 GTCTGCAGAG ATCTGAGGAA GGAAGGAAAG TGGGAAGGGG AAGGAAACAC TGACCCAGAG 960 GCACGGGCCC CTCCACACCT GCAGCACACC GACTCTCCAG ACATGAGTCT CTGTGGGAAC 1020 AGGAAGAGAC TCCAGAAAGC TGAGAATCGC AGACTGCCCA ACCGCAGGAG CGCTCCCAGG 1080 CTGGGGACAG ATGAGACAGC ATATCAACAG TGAGCCCCAT CGGCGGCAAG CTCCCAAGCA 1140 GCCCCAAGCC CAGAGCAGGA GAACATCCCA GGCTTTCCTC GAGCTGTCTC CATCCCCAGA 1200 GCCCACAGCC CTAATCCCAC TTCCAGCCAC AGGCAAACTC CTATTCATCC TCCAAAACCC 1260 AGCCCAGTAA TCCTGTGTTT GGAAACACTC GCCCCACCCC CCTGCAACTC TGAGTGACAC 1320 CCGGGCCCGC 1330
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