Tag | Content |
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EnhancerAtlas ID | HS017-01592 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr1:109966940-109968920 |
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) |
FOSL2 | MA0478.1 | chr1:109968717-109968728 | GGGTGACTCAG | + | 6.02 | IRF1 | MA0050.2 | chr1:109968238-109968259 | AAACAGAAACTGAAAGTAAAA | - | 9.95 | JUNB | MA0490.1 | chr1:109968717-109968728 | GGGTGACTCAG | + | 6.02 | Nkx2-5(var.2) | MA0503.1 | chr1:109967782-109967793 | AAGCACTCAAG | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr1:109967392-109967407 | GAGGTCAAAAGATCG | + | 6.19 | Nr2f6(var.2) | MA0728.1 | chr1:109967181-109967196 | GAGGTCAGGAGTTCA | + | 6.22 | REST | MA0138.2 | chr1:109967750-109967771 | ACCAGCACCTAGAACAGTGCC | + | 6.46 |
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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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Enhancer Sequence | GGTCAGCGCC ACCACACCCG GCTGATATTT TTTAATGTTT AGTAGAGATG AGGTCTCACT 60 ATGTTGCCCA GGCTGGTCTC CAACTCCTGA GCTCAGGCAA TCCTGCCTCG GCCTTCCAAA 120 GTGCTGGAAT TACAGGCATG AGCCACTGTA CCTGTAAACA ATTCTTTAAG AGTCTCAGGC 180 CGAGCGAGGT GGCTCTCGCC TGTAATCCCA GCACTTTGGG AGGCCAAGGC AGGTGGACCA 240 CGAGGTCAGG AGTTCAAGAC CAGCCTGGCC AAGATGAGGA AACCCTGTCT CTACTAAAAA 300 CACAAAAATT AGCCGGGCGT GGTGGCACCG CCTGTAATCC CAGCTACTCA GGACGCTGAG 360 TCAGAGAATT GCTTAAACCC AGGCGGCAGG CCAGGCGCGG TGGCTCACTC CTGTAATCCC 420 AGCACTTTGG GAGGCCAAGG CAGGTGGATC ACGAGGTCAA AAGATCGAGA CCATCCTGGC 480 CAACATGGTG AAACCCTGTC TCTACTAAAA ATACAAAAAT TAGCTGGGAG TGGTGGCGCG 540 CGCCTGTAGT CCCAGCTACT CGGGAGGCTG AGGCAGGAGA ATCGCTTGAA CCCAGGAGGC 600 GGAGGTTGCA GTGAGCCGAG ATCATGCCAC TGCACTGCAG CCTGGCGACA GAGCGAGACT 660 CCGTCTCAAA AACAAACAAA ACCCAGGAGG GGGAGGTTGC AGTGAGCCAA GATCACGTCA 720 CTGCACTCCA GCCTGGGCCA CAGAGCGAGA CTGTCTCAAA AGAGTCTCCT ATATGCGAGC 780 AAGGAGCTTG ATTTTGTCCA TTGCTGTAGC ACCAGCACCT AGAACAGTGC CTTGTTCACA 840 GCAAGCACTC AAGCACATTA ACTAAGAGAA TAAAAAGGGA TGTATTTTAG GCCGTCTTGG 900 GAAGACAGAA AAATAAGTAA CAAAGCAGTC AATACATATG TTAAGTAAAT GGCCACAAAA 960 TTTAATAAAT GCCTTCTGAT AAGCATAACA ATTTCTATCA TACACACCCT AACTCAAAAT 1020 TATGTCACCC GAAGATGATT CTCTTCAATG TTCTGGAAGT TAAATATCGA CCAACAAAGT 1080 CACTTTATAG GACAGTGGGG AAATATGTCA AAACTTCACA CACATCTTCT ACGAGTCAGT 1140 AAAAAAGATG AAAAAGTGGT AACTGCAGGT GGTAAAACTT CGACAGGATC AGCATATACT 1200 TGACAGGAAA TGCAGCATCT CATACCACTC AGTACAAAGA AAATGTCTGC CTTCCCTGAC 1260 TTTAAAAAAG AGTAGCTATG TAAAAACTTA ACTGACGAAA ACAGAAACTG AAAGTAAAAA 1320 TGTCTACAGC ATATATATGT ACAACTTAAT ATTGTGAACA TTTTCATACC ACAAAAGTTT 1380 TTTAAAACTT GCTTTAAACT TTTAAAAAGT CAGAAAAAAT TTTGGTCAAT TGGAATCGGC 1440 ATGATGAGAA ATCTCTTGAA AACCATTCTA AATTCCAGTT CCTATAAAAT CAGACTCCAG 1500 ACAATATATC CAGCCAAAGC TACGACTGCC TTCGCGCTTC TGAAGAAACT ATACACCGCA 1560 GCATGCCCTA CTACAAACCA GTTGCTTTTT CTTCCAGGAA GCACGTTTAA CTTTTTGTTT 1620 GTTTGTTCAA GGCAGTCATA CTAGGCACGA AAAGATGAAC GGAGCAAAGA GTGACCCTTG 1680 GCCTTCTCCG GGTTCAAGGT AGGAGTTCCG GCTCCTCACG CCTTCTTTAC CAAGCACCAG 1740 CCGGAGCTTC TCGCTTCCGC ACCGAGTTAG GACCCAGGGG TGACTCAGCG GTAGGACAAG 1800 TGCCGCCGAT GTGGTCTAGC TTGGGGAAGG ACGGCGGGCG CCTGAGGAGG GCATAACATC 1860 CCCAGGTCCG GCCAGTCTCG GGTTCCTGGG GAGCCCCATG ACACGGCAGA ACCCAGGCCG 1920 CGCGGCCAGG TCCCGGGCCT GCCCACCCAT AATTCCCACC CGACGTCCCC CAGCTGCACG 1980
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