Tag | Content |
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EnhancerAtlas ID | HS108-13857 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr15:78535510-78537540 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr15:78536638-78536653 | TGACCTCTGACCCAG | - | 6.85 | Nr2f6 | MA0677.1 | chr15:78536638-78536652 | TGACCTCTGACCCA | - | 6.37 | Rxra | MA0512.2 | chr15:78536638-78536652 | TGACCTCTGACCCA | - | 6.12 | ZNF263 | MA0528.1 | chr15:78535906-78535927 | AGAGGAGGTGTGGCAGGGGGA | + | 6.06 | ZNF263 | MA0528.1 | chr15:78536447-78536468 | GGAGGAGAGGGGAAGGAGGAG | + | 6.43 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr15 | 78535592 | 78536443 | chr15 | 78536445 | 78536529 | chr15 | 78536539 | 78536776 | chr15 | 78537096 | 78537176 |
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| Number: 1 | ID | Chromosome | Start | End |
GH15I078242 | chr15 | 78534541 | 78537219 |
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Enhancer Sequence | CCAGGGATCT CATCACGACA GAGCCACGCA GCTGAGGATG TCTGTTGCTA CCCAGGCTGC 60 ACCTTCCACG CTGGCTGCCC CTGACCTTAG GCAGTGGCCT GAGGCTGGGG AAGGAACACT 120 GGATTGAGAG TCAACAGGAC TTGGTTCCAG CTTGCATGAC CCTGGGGGAA GCCTCCACAT 180 CGCAGAAGCC CAGTTTCCTC ACCTGTAAAT GACTACATTG ATTGAACAGA AACCCAGTGA 240 GCACTTAGCC CAGATGGGGT CTGTGAATGT CACACCTGGA AGGGCTTAGA AACACTTCTA 300 GCATTCTGCC TTCCTTTTAG ATGAGAAAAC TGGGGCCCTG AGAGAGGAAA TAACCTGGCC 360 AGGGCGAGGG AGAGGACTTG TGGATTAGAC AGGGACAGAG GAGGTGTGGC AGGGGGAGGG 420 GATATGCAAA TTCCTTTCTC AGCGCCTGAG CACTAGCCTG GGAATACCTG GGAATAACTT 480 CCTCTGGCAC AGACCCCCAA CATCAGGGAC CTCAGAAAGC GGTATCTTTT CTGAATCTGG 540 GGACCCCTCC AGGTTCGGCT TGGGCCAGCG GATGTGGCTG GGAATGGGAA GCCAAGGCCC 600 AGGAGTCCTG GCAAACGGCC CAGACAGCCA GAAGCCAGGG CCAGCACAGG CTGGGGCAGA 660 TCAGTGCTGC TCACCAAGGG GCTGGACAGC CAAGCATGAA GAACTTGCTC CCCTGCTCAA 720 ACCCCATGTC CTACTTAATG ACAAACTTCT AAGGCCAGGA AATGGGGGGC TGGGGGAACA 780 TCTTCAGCTG AGCCAGGCTG GGGCCCTCTG AGATTCCAGC TGAGTGTTGC CCCCACCCTC 840 CTTGTTGATG TCCAGAGGGC AATTGCTGGG AAGAAAAGAG TGCCCAGATG AGTTTGCACT 900 CAGGTGTGAG AGGTGCTTCC TGGACTTCCA GAACAAGGGA GGAGAGGGGA AGGAGGAGAC 960 ACTGGTGTCC AGAGCCATGC CAGACATTCA CCTCCAAGGC TTCATGTGTG CTTCATGACA 1020 GTCCTGCCAG AAGGCATTAT TATAACCCTC CATTGTGCAA ATAGGGACCT GAGAGGGCTG 1080 CGGCATGCCA ACGTGCCATA GTAAGCCAGT TTCAGAACAT ACACAGGGTG ACCTCTGACC 1140 CAGGCCTCTT ATCTCCAGGG CCAAGGGTGG GGCAAGAGCT CAGAGGAGGG CTCTGCAGCT 1200 ATAGGGTGAT GAGTGCGTGG TGGTTGCATT GACCGTGGGA ATGGGCCTTT CTCTGCTTGT 1260 TCTCAAGGAG ACCAGAGGAA CTCATCGTGC AGGGCAGTTA CAGCTGAATG AATTCGTGCT 1320 CTTTTCTGTC ATGTTACCCA AGGCTCTAAA AAAGTTTTTT TTTCCTTCTC CCCAAACAGG 1380 AATTTGATCA CCCCAATAGA CCACTCTTGC CTGGTAGGAC TTTGGGAGCT TCATTATTTA 1440 TGAGGGTCTC TCTCAGGCAG AACCCAACCA GACCTTGCCC CCACTCCAAG ATAGAGCAAA 1500 GCCCCTATCA CAGCCTGGAG AAGAGCTGCC ATCCTGGATG CTTGGGAACA GCTGGAGTCA 1560 GCCTTGATCA GCCCTCTCTG AGGACTCAGG AGGGTCCTTG GCAAGAAGAG TCGTCCCATC 1620 CCCAGGAACC ATCAGCATCT CTGATGTCCT TCAGAGCCTG AACATCTCGG TAAAGAACAT 1680 TCACACTGCA GGGCCATGAA GGCCAAAGAG AGTGACACAA AGAGACACAA AGCCCTTTAG 1740 TTGCTACTTG AGGGCTGGGC CCAGGTAGAG ATTGCAGACA CCCCACCGCC TCCTCCCACT 1800 CCAGCTTCCC ACATTTATCT CCTCTGGGAA GCCTTTCTAG ACACCCCCAC ATTCCCCAAC 1860 TTCCTCATAT AGTCCATGGA GACTCCCCCA CCGCCTGCTA CTCTCAGCTA AACTGCCACT 1920 TCTGCTCAGC TTGGAGCCAC AGGAGCCTGG CTTCTCTGCT GGCCTCGTGG TCTGACCACA 1980 CTCAGACAGA TGCGCATGAA TAAATGTGAC CATGTATCCA TCCCTCCAAC 2030
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