Tag | Content |
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EnhancerAtlas ID | HS180-48356 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr8:142336730-142337980 |
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 | AGGGCCAGAT TTTGAAATGT AGCTGCAACA ACTGCCCTGG TAAACTTGAT TCACCCCACC 60 AGGCTGGGAG CCACCTTCTC CCGGAGCCTC CTTCTCCAGG GAGGGCTACA GCCCCCAGCC 120 CACTTGAAGC AGGGGTCCCA GCCCTCTTCA TCTGTAAAAT GGGGTGGAGA GTTTCTTTCT 180 TGGGGTGTTG TGGGTTGAAC TGTGACTCCC CAAATTCAAA CTGAAGTCCT TAGAATGTGA 240 CCTTATTTGG AGGGAGTCTC CACAGAGGTA ATCAAGTTGA ATAAGGTCGT TGGAGTGGCC 300 CTAATCCAAT GTGACTGTGT CCTTGGAAAA AGGGAGATTT GGAGACAGAT GTGCCACATG 360 AAGGAGAGGA TGGCCCTCTG CAAGCCAAGG AGGCAGGCCT GGAACGGACC CTTCCCTCTG 420 GCCCTCGGAA GAACCCAGCC TGCTGACACC TTGATTTCAG ACTTCTGGCC TCCGGAGCTG 480 TGAGGCAATA AATGCCTGTT GTTTCAGCCG CCCAGCGAGT GGAACTTTGT TCTGGCAGCC 540 CCGGCAGGTG ACAGGGGGTT GTTAAGGTTG TTTAGATGTG TGCGAGGCAC GGAGCGACGC 600 CCAGAAGACG AGGGCCTCCG GTGAGTGTGA GTGATTCCTA AACACGGCAC ACAGCCAACA 660 AAACAAGACA ACACCAAGAC CGGGTGTGAG GTGGGCGGGA AAAGCAGGAC TTGTAGTTGA 720 CCTCTGGGTC CTGGGGATGG GGGCGGGCAC CAGGCATCAT GATGGGTAGG AGCACAGCTG 780 AAGGCCGGGG CCCTCGGGGG ACACACTTAG CCCCCCTGTG CTTCGGTTTC CCCCTTGGCC 840 AATAGCACCC ACCCAAGGGG TTGGAGGATT ACCTAAGGCA GGGGTTGGCC AACTCTTTCG 900 GGAAGGGCCC AGGGAGTAAA TCTTTTCTCC TTTGCGGGCT GTGAGGTCTG TGTTGTAAGA 960 CTCACTTCTG CAGCTGCAGT TTGCACGCAG CCTTACAGCA GATGTAAAGG AGTGGGTGTG 1020 GCTGAGTTCC CAGGAAACTT GATTCGTGGA CACTGAAAGC AGAACTTCAT GTAATATTCT 1080 TGTTCTTTGG TTTTTGTTTT GTTTGTTTGT CTTTTGAGAC AGGGTCTCGC TCTGTCACCC 1140 AGGCTGGGAT GCAGTGGCAC CATCTTGGCT CACTGCAGCC TCCACTTCTC AGGTTCAAGC 1200 AATCCTCCCA CCTCAGCCTC CTTGGTAGCT GGGATTACAG GCTCACATCA 1250
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