Tag | Content |
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EnhancerAtlas ID | HS105-80029 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr8:142337010-142338000 |
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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH08I141326 | chr8 | 142336345 | 142338899 |
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Enhancer Sequence | ATAAGGTCGT TGGAGTGGCC CTAATCCAAT GTGACTGTGT CCTTGGAAAA AGGGAGATTT 60 GGAGACAGAT GTGCCACATG AAGGAGAGGA TGGCCCTCTG CAAGCCAAGG AGGCAGGCCT 120 GGAACGGACC CTTCCCTCTG GCCCTCGGAA GAACCCAGCC TGCTGACACC TTGATTTCAG 180 ACTTCTGGCC TCCGGAGCTG TGAGGCAATA AATGCCTGTT GTTTCAGCCG CCCAGCGAGT 240 GGAACTTTGT TCTGGCAGCC CCGGCAGGTG ACAGGGGGTT GTTAAGGTTG TTTAGATGTG 300 TGCGAGGCAC GGAGCGACGC CCAGAAGACG AGGGCCTCCG GTGAGTGTGA GTGATTCCTA 360 AACACGGCAC ACAGCCAACA AAACAAGACA ACACCAAGAC CGGGTGTGAG GTGGGCGGGA 420 AAAGCAGGAC TTGTAGTTGA CCTCTGGGTC CTGGGGATGG GGGCGGGCAC CAGGCATCAT 480 GATGGGTAGG AGCACAGCTG AAGGCCGGGG CCCTCGGGGG ACACACTTAG CCCCCCTGTG 540 CTTCGGTTTC CCCCTTGGCC AATAGCACCC ACCCAAGGGG TTGGAGGATT ACCTAAGGCA 600 GGGGTTGGCC AACTCTTTCG GGAAGGGCCC AGGGAGTAAA TCTTTTCTCC TTTGCGGGCT 660 GTGAGGTCTG TGTTGTAAGA CTCACTTCTG CAGCTGCAGT TTGCACGCAG CCTTACAGCA 720 GATGTAAAGG AGTGGGTGTG GCTGAGTTCC CAGGAAACTT GATTCGTGGA CACTGAAAGC 780 AGAACTTCAT GTAATATTCT TGTTCTTTGG TTTTTGTTTT GTTTGTTTGT CTTTTGAGAC 840 AGGGTCTCGC TCTGTCACCC AGGCTGGGAT GCAGTGGCAC CATCTTGGCT CACTGCAGCC 900 TCCACTTCTC AGGTTCAAGC AATCCTCCCA CCTCAGCCTC CTTGGTAGCT GGGATTACAG 960 GCTCACATCA CCACGCCCAG CTAATTTTTG 990
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