Tag | Content |
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EnhancerAtlas ID | HS059-26235 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr2:114449810-114452400 |
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) |
Stat6 | MA0520.1 | chr2:114450522-114450537 | CATTTCTTGAGAACT | + | 7.19 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 114451056 | 114451436 | chr2 | 114452101 | 114452155 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I113692 | chr2 | 114450241 | 114451930 |
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Enhancer Sequence | CAAGGATTTA TATACAGATA ATGCAAAGAA TTTGAACAGC TCAATAGTTA GAAGCTAATT 60 AAAAATGTGT AAAGGATTTT AGTAGACATA TCACCTAAGA AGATATATAA ATGGCTAACA 120 CATGAAAAAT GTTCCAAATA ATTAATCATT AGGGAAATGC AACTAAAACC AGAATAACGT 180 ACATTCAGTT CATACCCACT AAAATGCCTA TAATTAAGAG ATTGACAATA CCAAGTATTG 240 ACAAGTATGT GTTGGTAAGA TTTTAAAATG ACATAGTCAT TTGGAAAATA GTTTGAAAGT 300 GTGTTAAAAA GTTAAACCTG TACTTAACAA ACGATCCATC AATTTCACTC CTAAGTATCT 360 ATGAAGAGAA TTGAAGGTTT ATGTCTACCT AAAAGCGTAC ATGGGGGTGT TTGAAGCCAC 420 ATTATTCATA ATAAGTAAAA ACTGAAAATA ATTCAAATAT CCATTAACTG GTGCATAGAT 480 AAAGTAAACT ATCCATTAAC TGGTGCATAG TAGATCTGTA CAATGGAATC CCTAGCAGCA 540 GCGAACCAAG GCTTCAAAGT TCCCTAGTGG TTTCTTTGCC CTCACTGCTG CATGCCACAA 600 AAAGACCATG CTATGAAAAG ACCAACATCT CCAAGCATAG CTGTAGATGA CTTTGCTTTC 660 ACTTCTGGTT ACAACTGAAC TTACTCATTC TTTGTCTTCT AAAGAAGCCA TTCATTTCTT 720 GAGAACTTTT CTGGTGTTTG GTTCCAGAAT CTGTCTTTTA GATGACAATT TTTTTTCTTC 780 AGAGTTAGAC ACAGACTCCA TGGCATTTTA CTATATTTAT AGCGTATTTT TATTATAGTT 840 ATGAAATCAG TTTTTTTCTT TTTAATGGAG TTCTTTTTCA AGTTTGATTT TTTCTTTTTT 900 CTTTTCTTTT TTTTTTGTGT GTGTGTTTGT TTGTTGAGAC AGGGTTTCAC TCTGTCACCT 960 AGGCTGGAGT GCAGTGGCAT GACCTCAGCT CACTGCAACC TCCACCTCCT GGGTTCAAGC 1020 CATTCTCCTA CCTTAGCCTC CAGAGTAGCT GGGACTAGAG GTAGGCACCA CTACGCCTGG 1080 CTAATTTTTG TATTTTTTTG TAGAGACAGG GTTTCACCAT GTTGGTCAGG CTGGTCTTGA 1140 ACCCCTGACC TCAAGTGATC CACCCACCTT GGCCTTCCAA AATGCTGGGA TTACAGGCGT 1200 GAGCTACTAT GCCCAGCCCC GAATTTGATT TTATTATACC AATATTATCT TCTCCCCCTC 1260 CCACAGTTCC CCAAACACTT CTCTACACAC TCTGGTCTGG CACAGTTTCA AATTTGTGGA 1320 GTTGATATCT GGGGCTCCTA CTGGAAGGAG GATAAAAACA GAAGGAATTT GGCACGGGGC 1380 TCCTCCATCT TCCACGCATG CGGCATTTGT TCTGAGAATG TCAGCTCCCT CACAGTGCAT 1440 GTCAGAATGG CATGCCAGCA TGGGCCTCTG GTCTAGCACA CAGAAAGGGT GAAGAGTACA 1500 CATGGTGACC ATTGTCACTT TGCAGATTTC CTGCCTCCCA CTCACATGTC TGAGACCAGT 1560 TTTGCTACTG TTGCACCGCT AACCACAGAA GCCAGAAAGG GAAACGACTT TCTTTCTTTT 1620 CTTCTTTTTT TTTTTTTTTT TTTGAGATGG AGTCTCACTT TGTCGCCAGG CTGGAGTGCA 1680 GTGGCACGAT CTCGGCTCAC CGCAACCTCC AACTCCCTGG TTCAAGCTAT TCTCCTGCCT 1740 CAGCCTCCCA AGTAGCTGGG ATTACAGGCA TGCACCACCA CACCCAGCTA ATTTGTGTAT 1800 TTTTAGTAGA GACAGGATTT CACCACGTTG GCCAGGCTGG TCTTGATCTC CTGACTGTGT 1860 GATCCACCCG CCTTGGCCTG TCAAAGTGAT GAGATTACAG GCGTGAGCCA CTGAGCCCAG 1920 CCAGGGAAAA TAAGTTTTCA ATAGAGAATT TTCTATTAAG GAAGAGAGTG TTCTTTCAGC 1980 AAAGACAGGC TTTAGCCACA CCTGTTTTTA TAAGGATTTG AGGGGAGGGA AATATGCCAA 2040 GAGACAACTT CAGAAGTTTA TAAAGACAAG AGCGACCTCT CCAAAACAGC TAGGAGAGTG 2100 GGTCTTTAGT GGTGAGGTCT TCATCTCTGT CTGATCTCTC TAGGCTGAAG GAAAGATGTG 2160 AATTTGCTGT GAAGGGATAT TCTCCTCAAG GACACTTACC ATCTGTTTCC TGGGGATAGG 2220 AAGGTAAGTC ATCAGTGTCA AGAACCTTAC TGGTAAAACA ATAAAACAAT GTATTCATTC 2280 GGATTTGTGC TCTTTAAGTG AGAGGGGTTC TAGAACAGCC TTTCTGTCTG GACCCCTTGA 2340 TGGTAAACCA TCCCGTGTGA GGTCTGCTCT TTACTGTGTG GACGAGGCCA GGGCTGTTAT 2400 TTGACATCCG TGGCCACAGC CCACAGTCTA ACGTCGGCCA GCTCCGGTGT GATTGTACTT 2460 AGTACATCAG TAGTCATGAG AAAACTGGCT AAGAAAACAC AGAGCTTCAA CTGGAACAAA 2520 ATATTATACG TGCAACACCC ATGACCGTGT GGCTGTTTTA TCCCCATTGC TCCTTTCTTT 2580 TCTGCAGAAG 2590
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