Tag | Content |
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EnhancerAtlas ID | HS099-18421 |
Organism | Homo sapiens |
Tissue/cell | HSMMtube |
Coordinate | chr5:134348410-134350290 |
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) |
ELK4 | MA0076.2 | chr5:134348693-134348704 | CCACTTCCGGC | + | 6.62 | Gabpa | MA0062.2 | chr5:134348692-134348703 | GCCACTTCCGG | - | 6.62 | ZBTB7A | MA0750.2 | chr5:134348692-134348705 | GCCACTTCCGGCA | - | 6.39 | ZNF263 | MA0528.1 | chr5:134349720-134349741 | GGAGCAAGAGAGAGGGGAGGA | + | 6.86 | ZNF263 | MA0528.1 | chr5:134349717-134349738 | GAAGGAGCAAGAGAGAGGGGA | + | 7.1 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_26574 | chr5:134348484-134351223 | Esophagus |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 134348703 | 134348753 | chr5 | 134349979 | 134350203 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I135014 | chr5 | 134350021 | 134350170 |
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Enhancer Sequence | TACATCCGAC TGCTATCTAC TGAGCTATGC TGGGTGCTGG GGCTTCTATG ATGAGAAACC 60 CGTGGTCTCT CCCTGGCTCT CTTGGTGCTC ACAGTTTTGT AGGGAAGACA GTCATCCAGC 120 CACTGAGGAA GTGACAATCA TTGAATTCAG GGTGGGGGGA CTGCGTAGAG AGAATCAGGG 180 CCACATTGAG CATCATGAAA ACAGTGTGAA AGAAGGATGG CTCTTCAGGG TGAGACCTGT 240 TGAGGTGCTG TGGGGGAATC CTCTGAGGGC AGGAAATGCC TGGCCACTTC CGGCACGGAG 300 AGAGCTTTGT GTCCATGCCC TGAAGCTGGG CTGGGGTAGA TAGGGTGTTT GTGCCCCTCA 360 TGACAGGGGG AGTTGCTCTG GGTCTGACAG GTCCAGGGAT GACGCCAGGC TTGGGGCTTC 420 CAGGGGTGCT CTTGTGGGTG CAGCCCCATT AGTAGGGCAG GCAGGCCCCA GGCAATGGCT 480 CCAGTTCAGG GCCGGGGCAA AGCAGACATT GCCAGCTGCT CACACAGGGT GTGCCAACAT 540 AGCCATGGGA ACGCTAAAAC ATATCCAGCT ACTCTCATCA GGAATCCTTG GAATTGCTCT 600 AGGCATCTGA GAGTGAAAAA AAGATTTAAA AATTGGCCTC AGTGGGGCAA GGTAGAAAGT 660 GCCATGGTTT TGGAGTTGGG ACACCTGTGT TCCCTGTTAG GGAGACCTTG GGTAAAGTGT 720 CTGGTCTTTC AAGCCTCACC TATTTCCTGT GAGAAATGCG ATGATAAAAT GACTGGGTGC 780 AAGGATCAAA TCTCTGTAAG GTGTGAGAAA AGAGGTAGTC AACTCATGGT TCACCCTTCC 840 CCACTGTCAG CCCTGCGCCT CTGCTGGGGG CACGTGTAGT GGGCTGTGCT GGTCAGGGGC 900 TGAGAAGGAC AAGGCGAGCT TGACGCTGGT GTTGGTGGGG AAAGTATGGA GCTGAGAGCA 960 GGATGCAGAG GTCATGAACT ATACAGGGGT ATGAATGGGT CCCAGGATGG AGCTGGTTCA 1020 GAATAGGCAG ATGGCACGTC AGATCTGGAA GGCCTAGATC CCATGCCTAG GAAGGCAGAC 1080 TTTGGGCACA GCCACCAGGG TGTGGTGTGG GAGGGTGCAT TCGTCCATTT TGTGTTGCTA 1140 TAAAAGAATA CTGGAGGCTG GGCAATTTAA AAGAAAAGAG GTTTATTTGG CTCATGGTTC 1200 TGCAGGCTGT CCAGGAGGCA TGGCAGCACC TGCTTCTGGT GAGGCCTCAA GAAGCTCCTA 1260 CTCATGGTGG AAGGCAAAGC AGAGCCCGTG TGTGTCATGT GGTGAGAGAA GGAGCAAGAG 1320 AGAGGGGAGG AGGGCTACCA GACTCTTTTA AACAACCAGC TCCCGAGTGA ACTAACAGAG 1380 TGAGCTCTCA CTCATCACGA AGTGGGGGCA CCAAGCCGTT CACAAGGGAG CCGCCCCCAT 1440 GATCCAACAC CTCCCACTAG TCTCCACCTC CAACATTGGG AGTCACATTT CAACATGAGA 1500 TTTGGAGGGG ACACACATCC AAATTGTATC AAAAGGCAAG CTGACTTTAA GGGCACAAGA 1560 AGAAGGCTTT CAGAGAGCAG AGAGCTGGTG GGGGCAGAGG TGACGTTTAC AGGGCCGGCC 1620 CAGCACTGCT GGCAGAGCAA GCTGATGGAT ATTTGGCACA AAGTCACAAA GCAGCATTTC 1680 TGTTTGGCTC TATTCGCCTG CAGAGCAAAC ACGGCAGATT GGAATTCCCA CTTGGGCTCT 1740 CACCAACTCA AACAGGCTTG GCCAAGACCT TTAATTGATT TGCTTGGGGC AGAAGTGGCT 1800 CTGCTTACCC ACGCCTGGCT GTGGAAAGCA GGACCCTCCT CACCCTCCCC CGACCCTGGG 1860 ATCTAGTAGG GTTGACCCTA 1880
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