Tag | Content |
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EnhancerAtlas ID | HS118-00953 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr1:109966980-109968920 |
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 | AGTAGAGATG AGGTCTCACT ATGTTGCCCA GGCTGGTCTC CAACTCCTGA GCTCAGGCAA 60 TCCTGCCTCG GCCTTCCAAA GTGCTGGAAT TACAGGCATG AGCCACTGTA CCTGTAAACA 120 ATTCTTTAAG AGTCTCAGGC CGAGCGAGGT GGCTCTCGCC TGTAATCCCA GCACTTTGGG 180 AGGCCAAGGC AGGTGGACCA CGAGGTCAGG AGTTCAAGAC CAGCCTGGCC AAGATGAGGA 240 AACCCTGTCT CTACTAAAAA CACAAAAATT AGCCGGGCGT GGTGGCACCG CCTGTAATCC 300 CAGCTACTCA GGACGCTGAG TCAGAGAATT GCTTAAACCC AGGCGGCAGG CCAGGCGCGG 360 TGGCTCACTC CTGTAATCCC AGCACTTTGG GAGGCCAAGG CAGGTGGATC ACGAGGTCAA 420 AAGATCGAGA CCATCCTGGC CAACATGGTG AAACCCTGTC TCTACTAAAA ATACAAAAAT 480 TAGCTGGGAG TGGTGGCGCG CGCCTGTAGT CCCAGCTACT CGGGAGGCTG AGGCAGGAGA 540 ATCGCTTGAA CCCAGGAGGC GGAGGTTGCA GTGAGCCGAG ATCATGCCAC TGCACTGCAG 600 CCTGGCGACA GAGCGAGACT CCGTCTCAAA AACAAACAAA ACCCAGGAGG GGGAGGTTGC 660 AGTGAGCCAA GATCACGTCA CTGCACTCCA GCCTGGGCCA CAGAGCGAGA CTGTCTCAAA 720 AGAGTCTCCT ATATGCGAGC AAGGAGCTTG ATTTTGTCCA TTGCTGTAGC ACCAGCACCT 780 AGAACAGTGC CTTGTTCACA GCAAGCACTC AAGCACATTA ACTAAGAGAA TAAAAAGGGA 840 TGTATTTTAG GCCGTCTTGG GAAGACAGAA AAATAAGTAA CAAAGCAGTC AATACATATG 900 TTAAGTAAAT GGCCACAAAA TTTAATAAAT GCCTTCTGAT AAGCATAACA ATTTCTATCA 960 TACACACCCT AACTCAAAAT TATGTCACCC GAAGATGATT CTCTTCAATG TTCTGGAAGT 1020 TAAATATCGA CCAACAAAGT CACTTTATAG GACAGTGGGG AAATATGTCA AAACTTCACA 1080 CACATCTTCT ACGAGTCAGT AAAAAAGATG AAAAAGTGGT AACTGCAGGT GGTAAAACTT 1140 CGACAGGATC AGCATATACT TGACAGGAAA TGCAGCATCT CATACCACTC AGTACAAAGA 1200 AAATGTCTGC CTTCCCTGAC TTTAAAAAAG AGTAGCTATG TAAAAACTTA ACTGACGAAA 1260 ACAGAAACTG AAAGTAAAAA TGTCTACAGC ATATATATGT ACAACTTAAT ATTGTGAACA 1320 TTTTCATACC ACAAAAGTTT TTTAAAACTT GCTTTAAACT TTTAAAAAGT CAGAAAAAAT 1380 TTTGGTCAAT TGGAATCGGC ATGATGAGAA ATCTCTTGAA AACCATTCTA AATTCCAGTT 1440 CCTATAAAAT CAGACTCCAG ACAATATATC CAGCCAAAGC TACGACTGCC TTCGCGCTTC 1500 TGAAGAAACT ATACACCGCA GCATGCCCTA CTACAAACCA GTTGCTTTTT CTTCCAGGAA 1560 GCACGTTTAA CTTTTTGTTT GTTTGTTCAA GGCAGTCATA CTAGGCACGA AAAGATGAAC 1620 GGAGCAAAGA GTGACCCTTG GCCTTCTCCG GGTTCAAGGT AGGAGTTCCG GCTCCTCACG 1680 CCTTCTTTAC CAAGCACCAG CCGGAGCTTC TCGCTTCCGC ACCGAGTTAG GACCCAGGGG 1740 TGACTCAGCG GTAGGACAAG TGCCGCCGAT GTGGTCTAGC TTGGGGAAGG ACGGCGGGCG 1800 CCTGAGGAGG GCATAACATC CCCAGGTCCG GCCAGTCTCG GGTTCCTGGG GAGCCCCATG 1860 ACACGGCAGA ACCCAGGCCG CGCGGCCAGG TCCCGGGCCT GCCCACCCAT AATTCCCACC 1920 CGACGTCCCC CAGCTGCACG 1940
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