Tag | Content |
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EnhancerAtlas ID | HS196-01464 |
Organism | Homo sapiens |
Tissue/cell | ZR75-1 |
Coordinate | chr1:110777970-110779240 |
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) |
GATA2 | MA0036.3 | chr1:110779120-110779131 | ACAGATAAGAA | - | 6.14 | Gata1 | MA0035.3 | chr1:110779120-110779131 | ACAGATAAGAA | - | 6.62 | JUND(var.2) | MA0492.1 | chr1:110778708-110778723 | GATGACCTCACTTTT | - | 6.05 | Sox3 | MA0514.1 | chr1:110778878-110778888 | CCTTTGTTTT | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65653 | chr1:110775910-110779459 | Pancreatic_islets |
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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 |
GH01I110234 | chr1 | 110777486 | 110779509 |
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Enhancer Sequence | AGCCATTTGC AGCCAGGCTG GCCTTGGAAA AGCTTGGCCA GGCGATAATG GGACGGGATG 60 CGCTGCTGAC TCCATAATGA TATTACGCAT CAGGGCCCAC GGCCAAAGTG GCTGTTTTTT 120 CTGTAGATCG ATGTGGAACC ATTTCATGGT CAGGGGCTGA GAACCCAGCC AGCAGCAGGG 180 GTACTAGATG CCAGAGTGGT CCTGAGGGGA CTGAAGGGGT GGCAACTGGG GTCCCCAGTG 240 ACCGTTTCAG GCTGCTGGAA GAGGAGGGGG CAGTGTGCAG GAGGGTGGAG GGGTGGACGA 300 GAGAAGCAGC AGACTGCCCC TCCTCCCCAC CTCACAGAAA CAGCAGGCCG TGCTGTCAAG 360 GAAGAAAGGG CTCTGGCTTC CTCCTGTTCC CCAAAGCTGG AGTCGAGCCC AAGGTAGGGA 420 GCTGGTTAAA AGAACAGGAC ATTGTTTAAA AGAATAAGAC AGACTTTTGA AGTCAGGCAG 480 ACTTGGGTTT GAGTCCTGAC TCCATCACTT CCTTGTTGTG TGACCCTGGG CAAGTTACTC 540 AGCCTCTGTG AACGTCTATT TCCTCATCTT TTAAATGTAG TATCTGCCTG AGGCCGTGTC 600 TCTCTCATTG AGCCATGAGG AGAAATGAGT CGGCGCCTGT AAAGCCTCGC GCACAGTGCC 660 TAGCACATAA CCATTGCTAG AGGGAGAGGG GAGTATTTTG GGGCAACTCA CTCCAGTAAC 720 AGATGACCAG TTTGGTTTGA TGACCTCACT TTTCAGTGAA TCAGCCTCAT TTCACTGAAG 780 TCCTTAGTCC TTATCTCCTT GTGAAGGAAT AAGAGGGGAT GATTATACCT AACAGCGAAC 840 ATTTATTGAG TGCTGGGCAG TACATTTCAT GCTTATAAAG ATGCATTCCA AGATTGATGT 900 TATCCTTACC TTTGTTTTAC GAGGAGAAAA CCAACACAAC AATGTCAGGT CATTTCTCCA 960 AAGTCACACA GCCATTAAGT AGCAAAGCTG GGATTCAAAC TCAGTCTGGC TCTGTGGGTC 1020 CAATGCTTAG CCACTCTCTG AACTGAGTGG GGCTTGTGAG TCATAACCTC CAGTGTAGGA 1080 GTTTGTGCTT TTAGTGTTAT TTCCTTAACT GCAATTGATT CTCATAGCAA AGGTATTGTT 1140 TTCCCCTTTT ACAGATAAGA AACCAAGGCT TGGAGAAGTG AATCATTAAA CTCACTCTCC 1200 CTTTTACGTG TATGTACCCC ACCCCACACA CACATAAAGC GAGGAGGAAT GTCCTCTTGG 1260 GATTCATTCA 1270
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