Tag | Content |
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EnhancerAtlas ID | HS047-04956 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr10:116004560-116005910 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr10:116005099-116005117 | CCTTCTGTACTTCCTTCC | - | 6.47 | HNF1A | MA0046.2 | chr10:116005166-116005181 | TATAAATAATTAACA | + | 6.59 | HNF1B | MA0153.2 | chr10:116005167-116005180 | ATAAATAATTAAC | - | 6 |
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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 |
GH10I114244 | chr10 | 116004001 | 116007410 |
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Enhancer Sequence | GGTATAAAAA AGAATGCAGT GAACACAGTG AGTGCAATGA TGCCCTGAAA GGGTCCCTCT 60 AGCCCTCCCA CAGGAGGTAT TCTGGTGCTT TGTTTATCTA GCAAGCAAGG ACCTCCCCTA 120 CTATACATCA GGCACATGCA GGTCTCTGGA GCTCCAGCAG AGACTAGATA GTCTGTAGTC 180 TCAGGCATTT GCCGCCTGGC AGTCAAGACA AACGTATCAC TGGGCAGTTT CAGCGTGGGC 240 TGTGTGACAG TAGGGATTGT ATTGAGGGGG ACAGGGGAGG GAGGTGCTGC AGAAGTTGCA 300 GAGCCAACAC CGTCTGATTG ATCCAAACAG CTAGGAGAAG GCATTTGACA TCCTGTGTGC 360 ATTTGCAGAT TGCCAACATA CATTCTATTT TAATGAGCAG AAACTTGGGC GCCTCTGGAA 420 AAACATGCAG CTGGGCAAGC AGAGGCACAT AGTGGATCGA GATCAAGCTG CTTAAGTTGG 480 TCTCATAGCA CGGAGGGAAG GGGACTGTGT TTACTGGGTG CCTTCCTATG TGGCAGGAAC 540 CTTCTGTACT TCCTTCCACT TTATCCTCAC AGCAGCCTGG GGAGGTGGCT GCCAGAATCC 600 TTGTTTTATA AATAATTAAC AGGCCTGAGC CTCAGTCTCC TGCCAGTGCC CAGGGTCAGA 660 AGCTGTAACT CCGTAAAATC GTCCTGAACC TAAGGAATAG AGACAGCATT GAGAAGCTCT 720 TCACCGCATC CTCAATGCCT CGCCATTGCC TGACTCACAG GCGGCAGGTG GGGGCTTGTT 780 CTGCCTCTGT GGTGTGGAGT AAGAGGGAAA AAAAAAATGT CCTTAGGGGA AAATGAGTCT 840 TTCTTGCTGG CATGCACAGG GCTGGAAGCT AGCAGGAAGT ATGTGCTGCA GGCCAGTATC 900 CTTCTCACCA CCTTTCTCCC TTTGATCGTG TCTGTAGAGC TCCTGACATA CTGGCTCTTG 960 CCATGTTAGG TGTCTGATTT TCACTTAGAT CAGGAGAAGA CTTGAGCCTC TTAGTCATTT 1020 GAAGCAGGAA GACCCTGCAC GAAGACTCTC AGCTGGCAGG GACATTTGTT TTATAATAGT 1080 TTGTTTTAGG ACTGCTTTGA AATCCAAGGA GCTCTATAGA CAGTTCCAAG TGGTGCATAT 1140 TTTAGAATTA GGTAGAATCT GGTGGCATCA TGGAAATAAC CACACAGTCT GAGAATATTG 1200 GGTGGTCAGT ACATGCTCCA TCCTCCAGGA GGACCACTCT CTGTGGCACC CTGGACTACC 1260 TGCCCCCGCC CCCCGCCCAA GATGATTGGA GGTCAGATGC ATGGTGAGAA GGTAGATCTC 1320 TGGAGCCTTG GTGTTCTTTG CTATGAATTT 1350
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