Tag | Content |
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EnhancerAtlas ID | HS113-13818 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr16:24534010-24536270 |
Target genes | |
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) |
Foxd3 | MA0041.1 | chr16:24535532-24535544 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr16:24535536-24535548 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr16:24535540-24535552 | GTTTGTTTGTTT | + | 6.32 | Mecom | MA0029.1 | chr16:24535331-24535345 | GAGACAAGATAAAA | + | 6.99 | TCF3 | MA0522.2 | chr16:24536170-24536180 | AGCAGGTGTT | - | 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 |
GH16I024522 | chr16 | 24534223 | 24536408 |
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Enhancer Sequence | CTGTAATCCC AGCTATTCAG GAGGCTGAGG CAGGAGAATC ACTTGAACCT AGGAAGCGGA 60 GGCTGCAGTG AGCTCAGATC ATGCCACTGC ATTCCAGCCT GGGCGACAGA GGGAGACTCC 120 ATCTCAAAAA AGAAAAAAAA AAAAGAAGGT CCTTGAATAA TACATTGTTT CATTCAACAT 180 CAGTGGTTTC ACCATAACTC AATCGCCAGC CGGGGCCACT ATCTGGAATT CGCACACTCT 240 CCCCCCATCT GCATGGGTTA CCTCATTAGG TTTCCTCCGA CATTGTAAAG CTGTGCCTGT 300 TCGGGGAACC GGGCGTCTAC ATGGTCCCAG TGTGAGTGAG TGTGTCTGTG AGTGTGCCTT 360 GTGATGGAGA GTGTCTTGCC GGGATGGGGT CGCATCACGC ACCCTGGGCT GCCAGGACAG 420 GCTCAGGCCA CCCGAGACCG TGAACTGGAA TAAACAGGAA AATAACAATC TTACATGTTT 480 TTCTTAATCT TTCTTAAAAG TATGTATAGC TCACATTCAT TTCAATGTTC AATAGGAGAA 540 GTGTGTTGGT CTTTATTTAG AAGTTTGGTG ATGTTTTTCT GACCAGAAAT ATGCCGTAAG 600 AATTTAACTC TTGTTAATAT CAATAAACCT ATGGTAAAAC TGGTTTTGTT ATGTGTTGTT 660 TCGCTTAAAG TCACAGTTTC CAATAACCTG TTAATGACGT TAGGTGAGGA CTTACTGTGC 720 CTGAGATGGG CACTGGTGTG ACAGACACCA TTAGGAGCAC CTAACAGGGA GGGCGAGCTC 780 ACCCCCTGAG TTTGAACCCT GACTCCATCA CTATTAGCGG GGGCCCTGGA CCCACCTCTG 840 GGATATATAA CCTGAGGTTT CCTTCTGTAA GCCCGGGGTT TCTTCCTCTG TAAAACAGGG 900 AGAAGAATCA GGCCTCCTTC ACCAGGTCAT CACAAGGATA AGTGAGATAG TACCTGTTAA 960 GCCTGTAGTA CAGCACCAGG CCTATAGGAC CAGCAACCCC GGTTGCAGAG TTGGGGAGAG 1020 GAGGGCGGGG CAGATATTTG CTGGCAGCAT CACTCACAAA GCCTGAGAGA TGACCCAGAT 1080 GAGCGAAGGC TTCCCCGTCT GCACTTCGTC CAGGGAGGTT CAGCAGTGCG AGGGGAGACT 1140 CCAGGCCAGC ACTCTGCTTT AATCTATCAA GCTTGTCACT GCTGCGGAAG CCAGACAGAA 1200 CCACTTATCA AGAGTCATTC TGGGGCCCCA CAAATAATTC CCCAACCCCT GCCACGAGCT 1260 TAGGGAAGAC ACAGGTGAGG CAGACAAGGT CTGTGCCCTC TGGGAATCTT ATCTCAAAGC 1320 TGAGACAAGA TAAAAACAAA GATAATAGGA GACTCACTGT CGCAAGGGGA TATGTTGGTC 1380 TGTTTACAGA GGGCCAGCTC TGCTCCTGTT CTCCACGGGA AATGTTAGCC ACATGCAGGA 1440 AAATAGAGTT GGTGGAGTGG GGGAGACACT GCTCTCCCTG GCAAGACACA TCCCGTTTTC 1500 TTGGAGGTTT TGATGTTGTT TTGTTTGTTT GTTTGTTTGT TTGAGACAGA GTCTCACTCT 1560 GTCACCCAGG CTAGAGTGCA GTGGCAAGAT CAGAGCTCAT TGCAACCTCC ACCTCCTGGG 1620 CTCAAGCGAT CCTCCCACCT CCGTCTCCCG AGTAGCTGGG ACTACAGACA TGCACCAACA 1680 CATCCAGCTA ATTTTTGTAT TTTTTGTGGG AATGGGGTCT CACTGTTGCC CAGGCTGTTC 1740 TCAAACTCCT GGGCTCAAGC ACTTTGGCTT CCCAAAGTGC TAGGATTACA GGTGTGAGCC 1800 ACTGTGCCTG GTCTCTGGTT TAGTTTTGTT TTTATAATGT AACTTTTTTG TTGTTGTTGT 1860 TGTTGTAGAG ACAGCATCTC ACCTTATTGC CCAGACTGGT CTTGAACTGA TGTCAAACAA 1920 TCCCCCAACC TCGGCATCCT AAAGCACTGG TATTACAGGC ATGAGCCACC ACATCCAGCT 1980 CACATCCATT TTAAATGATG GCTCCTGTGT GACCTCAACT CTCTAAACTT CATTGCGTCA 2040 TCTATAAAAT GGGATAATAT TGGGATGGAT TCACAGTGTT GCTGGGAAGA TTTAAGAATT 2100 CAGTGCAGTA AAAAGTGTTT GGCTCAGGGT ATGGTGAACA GAAAATGCAT GGTAAATGCA 2160 AGCAGGTGTT GTTTTGTTGG TGTTAGGTTT ACCAAGTTGG AAGCACTTCA GAGAAACATG 2220 CCACATGAAT TTATGTCCCA AACAACCCCT AAGTGGTGCT 2260
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