Tag | Content |
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EnhancerAtlas ID | HS037-39982 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr9:36764850-36766650 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TCF3 | MA0522.2 | chr9:36765870-36765880 | AGCAGGTGTT | - | 6.02 | ZNF263 | MA0528.1 | chr9:36764863-36764884 | GGAGGAGGAGGTGGCAGGTGG | + | 6.25 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 36764861 | 36764955 | chr9 | 36765862 | 36766252 |
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| Number: 2 | ID | Chromosome | Start | End |
GH09I036764 | chr9 | 36764861 | 36764955 | GH09I036765 | chr9 | 36764998 | 36766650 |
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Enhancer Sequence | GGGAAGGAAT TTCGGAGGAG GAGGTGGCAG GTGGCAGGTG GCGCAGGTGG CAGGTGGCGC 60 CGGCACTTAG CCACCAAGGG TGGAGGAGGG CCTTCAGGAG GAGGAAACTA GCGGCGAGCA 120 GGGGGTCAGA GGAGGTAAAC GCTGTGAACA TACCGCCAAG TCCCCATGCT GGGGGTGCAA 180 AACATTGTCA TGAAGGATAA GATTGGGGGG CTAGCTAGGA CAAGATTGTG GAGGACACTG 240 ATTATCAAGC TGGAATTATG CAATTTCTGT CGAGAGCACC TGGTCACCAC CGCAGGTCTT 300 TAAGCAGCTA TGGATGGGAG GCGACCCTGG CAGCGGCGGG CGAAGATGAG TTAGAAGGGG 360 ACAGGAATGA GACAAGAGGA AGGGAGGGAA GAGACGAGGT GGGGAGGACG GGAAGGCGTG 420 CAGGGAGTGG GCCGGTGCGA GAGGGACATG GGATGGAGTC CACAGGGGAA GAGCTGGGGA 480 CTCCAGGTTT TCTGGTCAGG AGAGACTGGA GACGCCACTG ACAGAAAGAG GAGGAACAGG 540 TGTGGGGAGA ACTGATGTTT CTTCGACCAG AGCCATCTGC GGAAACATCG TCTCCTCCGT 600 GGGGCCCAGC TTTCATTCCT CACAGCAGTG ATCACTGCAT GGCAAACAAT CACATTCATC 660 TATTATTTGT TTCTTGTCTT TGCTCAATCA GCATATAAGA GAGTACGAAT TCCATCTGCC 720 GTGTTCACAG CGCCATCCCC AGAACCTACA ACAGTGTCGG CTTCTAGTAG GTGATCGCTA 780 AATATTTTTT GAGTAAATAA ACGAATGACT CATGTCGTGC TGGAGGGGGA CTGTGGGACA 840 AGCATCCAGG AGGACTGGAG ATCTCCAGGA GGGACGTCTG AGCAAACAAG AATGTCCCAC 900 ACGTGGAGGT CACTAAGCCC AGGCTGTGTC TGAGATGGTT CTAAGAGAGT AAGAGAGAAT 960 GCACAGAAAG AAACCGGATC ACCTCCTATG CCCCCAGCGC CTGCACAAAG CCTGGCACAC 1020 AGCAGGTGTT GCGTGTTGGT TGACTGAATT AATAGATGAA CCTGCTCTTC GGCGAGGAGT 1080 GAGACTTCCT GTGCATAAGG GGCTCGAGCA GGAAGACAGC TGGCCGAGAG CGTGCGCTGG 1140 GGTCCAGAAG GTTGCCTCAG CTTCACAGGT GCCCATGGGT AACGTGTTGT GGTTCCCCGG 1200 AGACTCTGGG CGGGAGGAAG TGGGACCATA GAGAGGGGCC CACTTGGGTA GAGCGTCTAC 1260 CTCCGAGAGG TGGAACTTCA TTGGGCGAGT GGGTAGCCAA TGAGGAAGCT CCCTGAGGAA 1320 GAGCCCGCCC CTGGAACTGG GCCGAGGCAC CGCCCCCGCG GAGGAAGCCC CGCCTCTCCC 1380 CGTCCCTAAC ACTGAGGCCC CAGAGGCGAA CTGTCGGGAC TCCCGGGCTG CTTGGTGGCC 1440 TGAGAGGCCC CCGAAGGGCT CTGGGCTGCG CCTTCATCCG CTGCTTTCCT GTGTGACAAC 1500 CCCAGACCTC ATCCTTCAGG GGGTCTCCAT TGCCTCAGGT TCCTCTTTTT TTCGAGACGG 1560 AGTTTCAGTG TTGACTCCCA GGCTGGAGTG CAGTGGCGTG ATCTCGGCTC ACTGCAACCT 1620 CCACCTCCCG GGTTCAAGCG ACTCTCCTGC CTCAGCCTCC CGAGTAGCTG GGATTACAGG 1680 CGCCCGCCAC CACGCCCAGC TAATTTTTGC ATTTTTAGTA GAGACGGGTT TCACCATGTT 1740 GGCCAGGCTG GTCTCGAACT CCTGACCTCA GGTGATCCAC CCGTCTGGGT CTCCCAAAGT 1800
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