Tag | Content |
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EnhancerAtlas ID | HS093-14652 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr18:77578920-77580610 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SREBF2 | MA0596.1 | chr18:77579141-77579151 | ATGGGGTGAT | + | 6.02 |
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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 |
GH18I079819 | chr18 | 77579801 | 77580830 |
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Enhancer Sequence | CGCCTGTGAG ATGCGGCCAT TGGTGACTAA TGTCCGAGAG GCATCAGGAC TCGACACAGT 60 GCCCAGTTCT GCTGGGGGCT CCACAAACAT TTGCGTGTTG AATGAGAAAA CAGACATCTA 120 AGAATAGCAT CAGGAGATGA AAAAAACAAA AATAAGGGAA GAAGAAAGAG CAGAGAGACT 180 CGTTCCGCAA CAGCAGAGGA GGCAGCAGCT CCACGGTAGC TATGGGGTGA TAGGACCCCT 240 CTCACTGCTC ACCAAGGCCG GCGAGGGCAC CCAGGACGTG TCAGAGGGAG AAGGCCGGCA 300 GCCTGCAGAG ACACCAGGCA GGCCCTACCC GGGTGCAGCC CAGGACACCA CGGAGCAGCT 360 CAGGCGGGCC AGCCTCAGCC CAGCTGGCAC AGGGAGGGCA GCCTCACCAA CCGAGGGACC 420 CTTCCTGGTG GCTGTACGGG TGAGGCTGAG CCTCAGGGCA CAGATTTGGG GGTCTCTAGG 480 GAGAGCTGTT GCTGCCAGGC CTGGGGTCCC CACAGCACCT GTCCCACCTG GCACCACCCT 540 GGGCACCGGA CCCTCCTGGC AGAAGGCATG CAGCTGGCAC TCAGTGTCCC TTCAGATCGG 600 GCTGTGTTGG GCCTGGGTGT CACCCATGGA CAATGTTCAC GCCGCGGGGT TTGTGTGAGC 660 CCCGTCCTCC CTACAGGTGA GCTGAGCGCT CAGCCAAGGA CCCGGCCAGG CCTCACAGCC 720 AGCAGGCTGC AATAGAGGCC GTCCACCTCC CCTACGGCTC CTCGGTGTGA CTGGGGTAAA 780 ATACACATCA CCTAAGGTAT TCCATTTTAA CTATTTCAAG TGGACAGTTC AGTAGCATGA 840 ATTCCAACCG CCGTGCTGTG CAGGCATCAC CACTTTTTGC CAAATTCTTC CATTGCCCTC 900 AACAGGAAAT CTGTAACCAC TAAGCAGTAA CTCCCCCATA GTGCCACCTC CAACCCCTGG 960 TAAGGTCCAC TCTGCTTTCT CTATGAACCC CGCTATTCTA GGGATTTCAT GTAGGTGAAT 1020 CACACAGTGC TGGTCCTCCA GTGTCCAGCT TCTCTCACTC AGCATAACGC TCTCCAGCTC 1080 CAGCCGCGCT CCGAGGAGGA GCTCCTTCCT TCTCCGAAGG AGGTGCGTGT CAGAACCTCC 1140 TCCTATTCTG TGTCTGGGCA GTGCCCTCGT GCAGGGTACC CCACACTGTG TGCGTCCACC 1200 CTCTGTTGGC GACACGTGGG CTGTCCCCAT CATTTGGCTA ATGGGACTGA TGCTGCTCTG 1260 AACGTCGGCG CTTGTATCCT CTGTTTGAGT CCCTGTTTTC ACTTCCTCCC CACCTTTTGG 1320 CTAATGGGGC TGATGCGGCT CTGAATGTCA GCACATGTAT CCTGTTTGAG TTCCTGTTTT 1380 CACTTCCTCC AGGCATGTTC TTAGGAGGGA AATGCTGAGC CAGATGTTGA TGCTGCTGCT 1440 TAACTTTTAG AGAGTCTGCC AAACTTCCAC AGCAGCTGAG CCATTTTCCC ATCGGCAATC 1500 CTGAGGGGTC CAGTATCTCC CATCCTCACC AGCACTCAGG ATGGTCTGTC TTTCTTATTA 1560 CAGCCATCCT GGCAGATGTG AAGCGATAGC TCATATCTGC ATTTTCCTAA TGATGAGTGA 1620 TGCTGAGCAT CTTTTCATCT GCTTGCCGGG CATGTGTGCA TCTTCTTTGG AGAAAAGTCT 1680 GTTCAAATGG 1690
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