Tag | Content |
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EnhancerAtlas ID | HS139-27879 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr2:16499070-16501540 |
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) |
IRF1 | MA0050.2 | chr2:16499903-16499924 | AGTCACTTCCTCTTTCTGTTT | + | 6.16 | SPI1 | MA0080.4 | chr2:16499906-16499920 | CACTTCCTCTTTCT | - | 6.51 | Stat6 | MA0520.1 | chr2:16500626-16500641 | AGTTCTCTGGAAAAA | - | 6.75 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 16499732 | 16499985 | chr2 | 16500147 | 16500473 |
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| Number: 2 | ID | Chromosome | Start | End |
GH02I016317 | chr2 | 16499238 | 16501050 | GH02I016319 | chr2 | 16501201 | 16501350 |
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Enhancer Sequence | GAGCACCTGC CCCCCACACT CCCCTTCTCT GAACTTCTAG GTCCTGGTAA CCCCACCTCT 60 TCCCTTTTGT TCCCTCAACC CTAGAGCTAG TAATGGCTCT CTCAAGTCAC AGATCTCTGA 120 GTAAATGCAG TGCTAATTTT AAAAAACCTT TTCAGTCTTC CCACACCTGT AGCACACATC 180 TCCTGTATTA AATCCCCTCT GGTTGGAATA ACCTCTCACG GCTCCTGGGT CCTCTCTGGA 240 CCCCGAATGA TTCAGGTCAG CTCAACCTGG GGAAGACCTT CTTGGGAAAG TGACAAAGCT 300 GAGAAGTGGA GAGTGAACAG GACACAGCCA GGCAAAGAGA GAAGGGAGAG TGCGGCAGGA 360 AGAAGGAAAA GGGTGTGCAA AGGCTCTGCG GTGTGAACAC ACTTCTGCCA TTACAGGAGC 420 CGTGAAAAGG CCTCTGCAGC TGGAGTGGGG GCAGTGTGGC ACCTGATGAG GCTGAAGGGG 480 TGTGCTGAGG GGAGCCTCAT AGGCAGGGCC TAGCCATGGT TGTATGTGGG GTGCCCTGTC 540 TTTCCTAGGG TGGTGCCATG GCACGAATGA CCTCTCTGAA GGTGTGTCAT GCAGTTCCCT 600 TGCCTGTGGG TCACAGAAAA CATTGGATCT AATCTCAAGA GTAGTGGATT TTGAATGGGA 660 GAGGTGCAGG GTGTGATTTG TATTTGTAAA GGGCAACTTT ACCTGCTGTG TAGAGAACAC 720 ATTGCAGCGA GGCCAAGTGG AACTGGAAGT GGTTGTAGCA GTTTGTGCAG GAAGAGATAG 780 GGAGGAATGG GGCCGGAGCA GCATGGGGCT CCCTGGCTCT CTGACCTGGA GGCAGTCACT 840 TCCTCTTTCT GTTTAACCAG CTATAAAAGG AGGAGGCTGG GCCAGGGCAA GGATTTTTCA 900 GCTGGAGTCT AAGTCCTCTG AGGGGGGTCT ATGGATGGGG GTCAAGGGGT GGGAGAGACT 960 CTGAGATTGT ACACAAATGG TTGGACCTAT GTCCACAGAT GCCTTTTTCC CTCAGGGAAA 1020 AGGGTTCTTG ACTTTCAGCA CATTCTCTGT GAGGTAACAG CCACAGAGTT TTAAGCCACT 1080 CATCTAACAA TCTGGAAAGG CACTTGCAGC TCAAATTGCC AATGGCTTGC GATTCTGGAC 1140 CTTCCCAGTG AGTCATGCAT TCTTAAAGTG TTCCTGCTGG CTGTTAAAGT TTGTGAGGAA 1200 GGGGAGGGGA CCCTGACACC ATCTGGAGGC AGGGTGACAT GCCCATGGAG CTGCTCCAAG 1260 CACAGGTACA GAGGTAATCC ACTCATGGTG GCCTTTCTGA GCAGCAGGCT GGAGGCACCA 1320 TTTCACTTGA TCATTGACAC AACCCAATGA GGCAACAGGC ATTGACACCC ACTTCGTTAC 1380 CTGTGCAAAG GCTCCCCGAG GCCACCACGC CACCCTACTC TCTCACATCA CAGCCAGGGC 1440 TGCCTTTAGG AGCGCCCCAT GTTTGCCTTC TGCCATCCCC ACCTTCCAGC GCTCCTCGCC 1500 CCTGACCAGT GCCCTCTGAC ACCTCTTTCC ATCTCCCCTC TCTTCGGAAA CAACGGAGTT 1560 CTCTGGAAAA ATAAAATGTA AAATCAGACT CACTCTCAGT CACACGAATT GGGGTCACTG 1620 TGTCCAATTT CCAAAGGGAA ATGTTAGCTT CATGCTGCAG TGAGACTGGA AATGCCATTC 1680 CTTTCTGAAA AAGTGGGTCA GGCACCAGAA CATGTTACAG GGACTGGGGT CTTTACAGGG 1740 CGCCCCTGGA ATCCCTGAGG GCAGGGCCAC AGCTGGCTCT CGCATGCGTG CCCACCCTGT 1800 GCTGCCGGCC CAGCCCACGG GCTCCATCCT CCAACCCAGG CCAAGGCAGA AAACCAGATG 1860 CCTTTCCTAT GTCTCCAGCG TGTCCCATCT TGCTAGGATT TTTCACATTT TTCTGTGGAA 1920 GCCCTTTATG GTCTGTGACC CTGGCCACTG CTGAGCCAAA AAGACAACAG ATTTATGGCA 1980 GGCCTGGAGA GCAACAATCC ATGGATGCAT TTTCCCTGCT TTCAGTCAGT AATTTATTTT 2040 TAAATGATCT TTCTGTTATT TATGGGTCTC GCTGACTCCG ATGGCCAGGG TGAACTGCAT 2100 CTTATCAGAC TAGCAAAACT AACTGGATTA AAGGGCATCC CTCACATGTC ATCAAAAGGA 2160 GGACTAAGAA CCCCGATGTC TCAGAAGTGC AGCTGAACTG GTTCATCTCC TTTTGTCCCT 2220 GAACAGCGAT GTGAGCTCAG GCCAATGCCT TTGGGCCATG GGGTCAAACC TTCGCGGCTC 2280 CTCAGTGTTG AGGGCACAAG GCATGACAGC CGACTTCCTG CCTTGTAAAG TGGGGCTCAG 2340 GACACCCGCC ACAGACGCTT ATAGTGACAG TAGGGGAAGT CGTAGGGAAC ACCTGGTACA 2400 TCTAATACTC AATAAATGCT ACCTGTGTGA TTATTATGGC CTTCTTTACC TTGTCCTCAT 2460 CTCCCCTCTG 2470
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