Tag | Content |
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EnhancerAtlas ID | HS053-14746 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr16:2974310-2976150 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr16:2974331-2974352 | AAAAAAAAAAAAAAAGTAAAA | - | 6.16 | RREB1 | MA0073.1 | chr16:2976038-2976058 | CCCCAAAAAAGCCCCACCCC | + | 6.25 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 2974886 | 2976028 | chr16 | 2974413 | 2974613 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I002924 | chr16 | 2974443 | 2976192 |
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Enhancer Sequence | GACAGAGCGA GACTCCATCT CAAAAAAAAA AAAAAAGTAA AAAGCCAGAA CCCACTAGAG 60 TCACTTACTT GCCAAGCATA TCAGCTATTG TGTAGCATAC GACCCATGAT CTTACTGGCT 120 TGAAATAATA GGAGTTCCCC AGTGAACAGG GTTCTGTGGG GTTCCCAGGC TCCTTCATGT 180 CTGCAGGCAT CTAAGAGACT GCTGGGCTGC AGGGTACAAG GTGGTTTCCC TGAATGTGGC 240 AGTGCTCTGC ACATGGCCTC TCCTACAGCT GCCTTCCCTG CAGACTCAGG GCCCTGGCCC 300 GTGAGGCGTG GGAATGTGTA CCCTACGCTC CTGCCACGCT GTGGGTCACG CAACCCCCCC 360 AGGCTAGTCA AGGTTCAGGC AGGTGGAGAC AAAGCCCGGT TGCTGAGGGG CCTGTGGACT 420 TTAACGGGCG GAGTGGCGGT GGGTCAGCAT CTACCATCCA AGAGCCTGAA CGGGCAAGAG 480 TGGGAACGGG TCCTCAGCCT TCCACAAGCC GGCGGTCAGG GCCTTTTCTT GTATTGGAAC 540 TTTTTCCAGA TCTGTTGAAG CACATGTGTC TTGGAAGCCC TTTAAACAGA AGTGGGAAGT 600 GGTCGCCAGA GGACTGCGCT CTCTCCTGTC ACTTCCTGTG ACTCGGGTAC AGCTCCATGG 660 GAATGTGGGG CTTTCCTTGT CAGGCCAAGC TTGACGCAGT CCCCACCTTC ACTCTGACGG 720 CCTGGGACAG GCCCCTGCCC GCCTGCACTC CCATGGCGCA GCTGTGTCCT GCAGGACCAG 780 CTGGCGGGGT GAACAGTGTG CGAGTCACTG TGCCAGCCTG CATAGTCTGG GAGGCCTCTG 840 TCAGGAGCAA CCTGGCGTCC CCATGCCTCG CCCTGGCTGG GAGGGAGGCC GGGAATCACG 900 GCAGTTCTCA GGGAGGTGCC TCCCCAGGAA CAAAGGGGAC TTTCTCCAGA GGGCGGGGGC 960 CTCGCGGGAC CTGGGCTGGG GGGACCCCGG GAGGGTGCAG GGTCAAGGAA CTGCCACGTC 1020 CATCGTCCAT CCATTCCCAT ACATCCCGGT TCATGCTGTC CTGCCTCGTC CTGCCCTCAT 1080 CCTCATCCTT CCTGGTTTAG CCTCACCCGG TCCCACCCGG TCCCACCCAG TGCCATTCAG 1140 TCCCACTCAG TCCCACTCAT CCCCATTCAT CCCTGGAGCT CAGAGCGAGG GAGCGGGAGG 1200 GGCGGGCTGC CGGTAGAAGG ACTTGTGCCC AGGCCAATCA GCGCGCGCGG GGTAGGGGGA 1260 GTTGCGGGGG GAGGGGGGTA CGGGGCTTTC CGCCCTAACC TTTTCCTGCC TGGAGCCGCT 1320 CTGCTCGAGA GGCGCCTGCG AAGTCAGCTG GGGTTGCCCC TGCACCTCGT GTCACCCTGT 1380 GGGGCGGCAT GAGTAGGCCC AGAAGGACGG CATGGAGGAA CAGGCTGGGC CGGGGCTGGG 1440 GGAGGTGTGG TGGGACTGGC CCTCCTGGTA CCTGTGATTT CCTGGGGACC GGGCCTTAAT 1500 GGAGTTAAGG AGCCGCTCCC CTCTGCGTTG TCTCCGGAGC CGACCAGGCC TTCGGGAGTG 1560 GAATGTGGGG CCCCAGGCCA GGGAACTTTG GATCAAAGTG GGAGACCAGT GGGAACTGGA 1620 GCTGCAGCAT GTGAGGTGGG GGTGAGGACG CTGAAAATGT CAGGGACTGC AGTCTCGATT 1680 CCAGGCTGAG AGGTGGGAAA GACCCCACCA TCTGCCCACA CTCAGTTGCC CCAAAAAAGC 1740 CCCACCCCAC ACCATGACTG CCACTGACTG CCCCCAGGTC CCTGCCCCAT TCCCCATTAT 1800 TTGCCCTTTC TGCCTCTCCA GGCTGGAACC CGTGGTGACC 1840
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