Tag | Content |
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EnhancerAtlas ID | HS108-19582 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr19:11045520-11047780 |
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) |
CTCF | MA0139.1 | chr19:11047490-11047509 | AGACCAGCAGAGGGCATCA | + | 6.05 | Gata1 | MA0035.3 | chr19:11046192-11046203 | TCCTTATCTCT | + | 6.02 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH19I010936 | chr19 | 11046961 | 11047876 |
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Enhancer Sequence | TGAGACGGTG TGTGCCTGTG GTCCCAGCTA CTTGTGAGGC TGAGGTGAGA GGATCCCTTG 60 AGCCCAGGAG TTTGAGGCTG CAATGAGCTT GGTCATGCCG CTGCACTCCA TCCTGGGCCA 120 CAGAGTGAGA CACTATCTCC CCTCTAACCC CCAAAAATGA AAGGAAACAA AAGACGTCGA 180 GATGATACTA ACTAAATGCT ATCTCTACAC CATTACCTGC CAAAAATCTC TGTCCCCAAA 240 TCTGCCCTCT GTTAGACATT AGCCAACTTC AGGGAAGGGT TTTAAGGTGT CATCAAAGAC 300 ACTTGTTTCT CATTGATCAG AAGTATTGGA AAGGGTCCAC ACCATCATTG CTTGAGTCAG 360 TTATTAAATG CCACTTTTGA CTTCTCGCCA GGGTGTGTTC CAGGAAGATC ATCTGAAGCT 420 GCTGGGAGCT TGAAGCTGAG GGCAGTGGTC GGCGCTGTTG GTAGGAATTG TGGAGCTTGG 480 GCAGCCTGAA GGCTTTGTGT CTTGGCTTTG GGCAGAGGGT CAGCTTTTCC CAGAGGTCTC 540 ACTGTACTTC AGCCCATGCT CTGGTGTAAG GCAGAGGACA GGAGGCATAA GTGGGCTTTA 600 AAGCCAGGAT TTGGAACTCA GCTTTTACAC TTCCTTGCTT TGTGAGTGAA GTCACTTCTC 660 CATGCTTTGG GCTCCTTATC TCTAAGTGTG GGCTTGTCAG AAAAATTTAA AAGCCCACTA 720 AAGCACTTGG TACAGAGTAG GCATTCACAG TCTGTGGTGC GGCTGTGCAG GGAAGATTAT 780 GGCTCCGAAT CCATGCTGTG ACCTTCCTAA GTGGTTGTGG AGGGGCTGAT GCACCCTGCC 840 TAGTGGTGCA GGGCCACCAT GTAGGGAGGG CCCAATGTCT GATAGGATAG AGCCAAGGCA 900 CGCTTCTTTC TCAGATCCAA GTGACAGCCG AATCTAATAT GAACATTTCT GAGTTCTCCC 960 CCACACCTTG TTTTCAGGGA CGGTCTCACT CTCTCTCCCA GGCTGGAGTG CAGTGATGCA 1020 ATCTCAGCTC ACTGCAACCT CGACCTCCCT GGACTCAAGC TGTCCACCCA CCTCAGGCTC 1080 TCAAGTAGCT GGGACTACAG GTGTGCACCA CCATGCCCAG CTAACTTTTG TGTATTTTTT 1140 TTGTAGAGAC AGGGTTTCGC TATGTCACCC AGGCTGTTCT CGAACTCCTG AATTCAAATG 1200 ATCTTCCCAC CTCGGCCTCC CAAAGTGCTG GATTACAAGT GTGCATCACT GCACCCGGCC 1260 TGAGTTCTCC CTTGAAAAAA AAGGCGGGGG CGGGGGGGAG CAGTTTGGAG ATAGGGTCTC 1320 GCTGTGTCAC CCAGGCTGGA GTGCATTAAC GACCCATTGC AGCCTCGACC TCTTGGATTC 1380 AAGCAATCCT CCCACCTCAG CCTCCCAAGC TGCTGGGACC ACAGACACAC ACCACCACAC 1440 CGGCTAATTT TTTAAGTTAT TTGTAGAGAT GAGATCTCAC TGTGTTGCCC AGGCTGATCT 1500 CAAACTCCTG GGCTCAAGTG ATTTTCCTGC CTCAGCCTCC CAAGGAAATA AAATATTCTT 1560 GGATTCTTGG TTAGCTTTAA TTATTTCCGC TTTCCAGGCT AGCCCAGGAG TTGCCCTCCA 1620 GCACGTCCTT TGAAAAGTAC TTTTCGGCCG AGCGTGGTGG CTCACGCCTG TAATCCAAGC 1680 ACTTTGGGAG ACCGAGATGG GAGGATCACC TGAAGTCAGG AGTTGGAGAC CAGCCTGACC 1740 AACATGACGA AACCCTGTCT CTACTAAAAA TACAAAAATT AGCCGGGCAT GGTGGTGGGC 1800 GCCTGTAATC CCAGCTACTC AGGAGGCTGA GGCAGGAGAA TCACTTGAAC CTGGAAGACG 1860 GAGGTTGCCG TGAGCCAAGA TGGTGCCATT GCACTCCAGC CTGGGAGACA GAGCAAGACT 1920 CCGTCTTAAA AAAAAAAAAA AAAGTATCTT TCCCACTGTT GTGATTAGAA AGACCAGCAG 1980 AGGGCATCAG AGACTTAGTT CGGAGACAGA ACGTAGCTGA TTCCATCCTG CCTTACTTAG 2040 CCCCCATGGA ATGGCTCAAC GCAGGTTCCT TTTGTCCGCG GGCAGCAGCA AGTGGAGGTC 2100 GTGCAGCTTC CACTTGCACC AGTTTACTGT GCCTTGGAAT TGGATAGATG ATGGCAGAAG 2160 TCGAGGCCCC ACGGAGGGGC CACCTTCATC TCTGGAACCT GCACCTTTAC CTACTTATGT 2220 CCACAAAAAG AGTCAGACTC TGAATCTTTT TTTGTTTTTT 2260
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