Tag | Content |
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EnhancerAtlas ID | HS108-15974 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr16:89709060-89710830 |
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) |
EWSR1-FLI1 | MA0149.1 | chr16:89709470-89709488 | CCCTCCTGCCTTACCTCC | - | 6.31 | MEF2A | MA0052.3 | chr16:89710068-89710080 | ACTAAAAATAGA | + | 6.27 | MEF2B | MA0660.1 | chr16:89710068-89710080 | ACTAAAAATAGA | + | 6.32 | MEF2C | MA0497.1 | chr16:89710066-89710081 | CTACTAAAAATAGAA | + | 6.57 | ZNF143 | MA0088.2 | chr16:89710375-89710391 | CAGTGCATCGTGGGAA | - | 7.84 |
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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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Enhancer Sequence | AAAGGCAGTG TGCCAAAGCC AAATTTTCAG AGAAGCTACA AACGAGGGGA GGCTGGACCG 60 AATCGTACGG AACGGTGTGC ACCTGTGGCT CCAGGGCACG CAGAGGGGTG TACCACTGTG 120 CACCATGGCG GCTGCAGACG CCTCTTGGCC AGCGGCACAC AGCACTGAGG CCCACGGTTT 180 GTACCCAGGT CTTGGTTTTC TGGTTGGTTT TTTTGAGACA GGGTCTCACT TTCTCACCCA 240 GGCTGGCGTG CGGTGGTGTC ATCCTAACTC ACTGTAGCCT CAACCTCCCA GCCTCCCAAG 300 TGACTGGGAC CACAGGGGCA TGCCATCATG CCTGGCTGAT TTTATTTTTT GTAGAGATGG 360 GGGTCTCACT ATGTTGCCTA AGCTGGTCTC CAACTCCTGA GCTCAAGGGA CCCTCCTGCC 420 TTACCTCCTG GAGTGCTGGG ATTACAGGCG TGAGCCACCA CGCCCAGCCT CCAGATCCTG 480 GTTTTCTAAA TACCATTCCC CACTCGAAGG AATTGGAGCT TCCTGGAGAA AGGGCTGCTT 540 CCAGGGCTGG GGCAGGGAGA GACCAAGATA AGCCAGAGCC TCCTGCAGTG CTGGGAGTCA 600 GGCCGTGCTC AAAGACTGCC AGGGTGGATG GAAAGCTGAC CTAAATGCCC TCAAGACGAC 660 ACCACCTGAG CCACAAAGTC AGCAACAGCA ACCATTGTAG CCCACGCAAT AAACAAACAG 720 GTCCAGACTG ATAGAAATAA TGGAGTGGGG AGGGGTCCTC CCTAGAATCC CAATAGAACC 780 AGTGATTTCA TTTGTGTCGA TGGACACTGA CACTCAGGGC AAAGTGGGTC GAGGTTTGCA 840 CAGTCTTCAA CAATCTTCCC ACGAGGCACA TGAATTAAAA AGGGAAAATA CGGCCAGGCA 900 CAGGTGCTCA CGCCTGTAAT CCCAGCACTT TGGGAGGCTG AGGCAGAGGG ATCACCAGAG 960 GGCAGGAGAT CAAGACCAGC CTGGCCAACA TGGCAAAACC CCATCTCTAC TAAAAATAGA 1020 AAAAATAGCC AGGTGTGGTG GTGGGCGCCC GTAGTCCCAG CTACTCAGGA GGCTGAGGCA 1080 GGAGAATCGC TTGAAACCGG GAGGCAGAGG TTGCAGTGAG CCAAGATGGT GCCACTGCAC 1140 TCTAGCGTGG GCAACAGAGC AAGACTCTGT CTCAAAAATA ATAAAAAGGG AAAATGCTAA 1200 CTTCACAGTG GAGAAGCCTG GAGATGCCAC TGCACCCAGT GGTGAAGGTC ACAAAGTCAC 1260 CAGCACCGAG ACACAGGGAC ACCACGCCCC TGCCACCGAG CAGTCATGAA GACCCCAGTG 1320 CATCGTGGGA AAACCGCACC CCCCCAAGCT GAGGAGCATT CTGCAAAATA GCAGCCAGCA 1380 GGTTTCAAAC CATTCAGGTC ATGAAGAAAA CCGGGGAACC CTCCCAGATT GGAGGCGGCA 1440 GCACAAGGAC GTGCAGCAGG GACGTCAGAC CAGAGACCGT CAGGAGCACC ACAGTGCCCA 1500 TCAGACCAGA GGCTCAGGGG GACCACGGTG CCCAGCAAGC ATCCTGGTTT GGCCGAGGTG 1560 CACAGAGACC ATGTACTGTG CAACTGTTAG GCAAGTTTTA AATTATTTCA AAGTAAGCAG 1620 AGAACTGAAC ATGGGAGATT GTCGGTTTGG ATGGGGCCCG AGAATGAGCA TAGCCATCTG 1680 CCCAGCCCCT AGCAGTGAAC ACTCCAGGAA CCCCTCCTCA GCTTGGGGGA GATGGCCACA 1740 TCCAGGGGCT CACCCAAGGC TCCAAAGCAA 1770
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