Tag | Content |
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EnhancerAtlas ID | HS093-30747 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr8:142336980-142338100 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr8:142337742-142337753 | TGGGTGTGGCT | - | 6.14 | PLAG1 | MA0163.1 | chr8:142337516-142337530 | GGGGCCCTCGGGGG | + | 7.52 |
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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 |
GH08I141326 | chr8 | 142336345 | 142338899 |
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Enhancer Sequence | AGGGAGTCTC CACAGAGGTA ATCAAGTTGA ATAAGGTCGT TGGAGTGGCC CTAATCCAAT 60 GTGACTGTGT CCTTGGAAAA AGGGAGATTT GGAGACAGAT GTGCCACATG AAGGAGAGGA 120 TGGCCCTCTG CAAGCCAAGG AGGCAGGCCT GGAACGGACC CTTCCCTCTG GCCCTCGGAA 180 GAACCCAGCC TGCTGACACC TTGATTTCAG ACTTCTGGCC TCCGGAGCTG TGAGGCAATA 240 AATGCCTGTT GTTTCAGCCG CCCAGCGAGT GGAACTTTGT TCTGGCAGCC CCGGCAGGTG 300 ACAGGGGGTT GTTAAGGTTG TTTAGATGTG TGCGAGGCAC GGAGCGACGC CCAGAAGACG 360 AGGGCCTCCG GTGAGTGTGA GTGATTCCTA AACACGGCAC ACAGCCAACA AAACAAGACA 420 ACACCAAGAC CGGGTGTGAG GTGGGCGGGA AAAGCAGGAC TTGTAGTTGA CCTCTGGGTC 480 CTGGGGATGG GGGCGGGCAC CAGGCATCAT GATGGGTAGG AGCACAGCTG AAGGCCGGGG 540 CCCTCGGGGG ACACACTTAG CCCCCCTGTG CTTCGGTTTC CCCCTTGGCC AATAGCACCC 600 ACCCAAGGGG TTGGAGGATT ACCTAAGGCA GGGGTTGGCC AACTCTTTCG GGAAGGGCCC 660 AGGGAGTAAA TCTTTTCTCC TTTGCGGGCT GTGAGGTCTG TGTTGTAAGA CTCACTTCTG 720 CAGCTGCAGT TTGCACGCAG CCTTACAGCA GATGTAAAGG AGTGGGTGTG GCTGAGTTCC 780 CAGGAAACTT GATTCGTGGA CACTGAAAGC AGAACTTCAT GTAATATTCT TGTTCTTTGG 840 TTTTTGTTTT GTTTGTTTGT CTTTTGAGAC AGGGTCTCGC TCTGTCACCC AGGCTGGGAT 900 GCAGTGGCAC CATCTTGGCT CACTGCAGCC TCCACTTCTC AGGTTCAAGC AATCCTCCCA 960 CCTCAGCCTC CTTGGTAGCT GGGATTACAG GCTCACATCA CCACGCCCAG CTAATTTTTG 1020 TATTTTTAGT AGAGACGGGG TTTCACCATG TTGGCCAGGC TGGTCTTGAA CTCCTGACTT 1080 CAGGTGATCT GCCTGCCTCA GTCTCCCAAA CTACTGGGAT 1120
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