Tag | Content |
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EnhancerAtlas ID | HS047-18664 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr2:29247240-29249710 |
Target genes | |
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 | chr2:29247336-29247354 | GGAGGGAGGGAGGGAAGC | + | 6.16 | EWSR1-FLI1 | MA0149.1 | chr2:29249346-29249364 | GGAAAGAAGGAAGAAGAG | + | 6.25 | EWSR1-FLI1 | MA0149.1 | chr2:29247312-29247330 | TGAAAGAAGGAGGGAAGG | + | 6.55 | ZNF263 | MA0528.1 | chr2:29247329-29247350 | GGTGCAGGGAGGGAGGGAGGG | + | 6.87 |
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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 | GTATGTGGCT GCCTGTTGTC TGAGGGGCGG GGAAGTCAGG GAAGGTAAGG CAAGGGGAGA 60 GGCCCTGGGA TGTGAAAGAA GGAGGGAAGG GTGCAGGGAG GGAGGGAGGG AAGCAGGCAA 120 GTGAGGCTGC AGGGGGTCCC TTGAGATGCT AGAGGACAGG GTGATGGGTC AGAGGTTCTG 180 AGTGAAGAAG GGGCCCATCT CAGACTTCAC AGCAGGTGCT TCCCACTTAG CTGGGGGAGG 240 AAGACCCCTG CTTCCCTGTG CCGGGCATCC GGCTTCTCTC CCAACCTTTC ATCGGCCAGG 300 CCGGGGGAAT GCAGGGACCT CTGGCTGGAA GAGGAGGGGG CCGTTGCACT CCAAGGCTGG 360 GGAGCACACC GTGGCTGTGG GAGCGCCCCG GGAGACAGGG CTGCAGAGGC AGCCTGAGCA 420 TGGGCCCTGG AGCTCCTGTC ACCCCCAGGA GCAGTGTTGC TTTCTGATGA AATGTGGGCC 480 AGTGAGAAGA GAAAGTCGCA AAATTTCATT CTCCAGCTTG CCCCACTGGA CCTGCTCCTG 540 GGGAGGGGAA GGTATTGGGT TCCTGTTGGA GCCTTTCTGC AGATTTGTTT TCCCTGTCAT 600 TAAACACCCA CACTAAAAGC AAAACCAAAA GCATTTCCCA AGCTGCTTCT CCCGCACAGC 660 AAAAGGCCTC TCCACCCCAT AAGTGGATCA TTACACTGAT GCGTGAGGTT TCTCAGTAGC 720 CCCAGGGGCC TGTTGGACCA GCTGGGAGAC CTTTAGTAAT TGCACCATAG CATACTGCAA 780 AGGGTGAGAT CCTGCCCAGC CACATTGCCT GGGTTCACAT CCTGATTGTC ACTTCACTTC 840 TCTGTGTCTC AGTTGACTCA TCTGTAAAAT GGAGATAATA ATGGTGTCTA CCTCATGAGG 900 TTGTTATGAG AGGTAATTGA ATTGACTCAC GAAAGCGCAC TTAGAAAGGT GCCTGCCCAT 960 TCCTGACATT CACTGAGTGC TTACTGTGTC TATAATTAAC TTAGGAGAAA TGAATTGTAT 1020 TTTTTTTTTC TGGATGCCTC CCTTTGGCTC AGCTTCCTCA CCTGCAGAAT AGTGATGATA 1080 ATAGTAGCTA ATGAGGTAGA TGTGAGATAA TGGATAAAAG GTGCTGGCAT GGAGGGACAG 1140 GCAATTGATC ACTGTCAACA AGAACCAGGG TCATGGCTTG TGCATCTGAG TCCGCTGGGA 1200 TCTTGCTGAA ATGCAGATTC TGGTTCAGAT GTCAGTGCTG CTGGTCCATG GACCATGCTG 1260 AGTAGGGAGA GTTCTGATGT CCCCCACTGT GTTCCACTGG GGTGAGACTC TAGGGGACAA 1320 AAGGGTCAGT GCTTCCTGAT GGAGTGTGGA CACAGAGGCC CTTAGAAAGA GGTGCCATTC 1380 TGACAGGTTT CTCTTATAGA GCTCAGGTTC CACTTGTTAT GGTCACCAAC TCACCCATGA 1440 ATCCCTCTTC TCCCTCCTGT CTCAGTTCAG TTCAGCAAAC ATGCATTAAG CTCCTGCCAA 1500 GCACCAGGGA TGTGTCAGGC ACAGCAGGGC AGTGGGGTTG CCACAGAGAG GGAATCAGGA 1560 CTCCAGCCAG GACACTAGGT AGGGAAGCAC CAGGGGCCTG GGGCGGAGAA GGCAACCAGC 1620 CAGCCCCGAG GGGCCTGGAA CATGCAGCTC AGCTTCCCTG GGATTCTGCA GAGGGACAGG 1680 CAGGTGGATG AAAGCTATGT CCTTCAGCTC TAGTCCCATC CCTTCCGTCA AGCCAAGCCC 1740 ATTCAGCAAG GAGTCCTTAC TCCCTGCCTC CACTTTCTTG CCTTCCATTT CCCCTCTGCC 1800 CATCGAGTGT TGCTCTTGTT TCTGCCTCAC CCCAGTACTG TTCTCTGTAC ATTCAGGCCT 1860 TTTTTTTCTG GAGATACTTA ATGATCACTC TTTTCGTCAT TATGGATACA GCAGTGAAAA 1920 AGAAAAATGA AGCCCCTGTT GTTTTGGAGT TACTTCCTAG TCAAGGGAGA CAGATAACCT 1980 GGTCCCCGCC CACAGGGAGC TGGCAGCCTG ATGGGGGCCC TAAGGGTGCA ACTGTACTTC 2040 CCCGGGGACA AAGACAGCGC TACCTTGGGC AGTGGGTGGG ATGTCTAATT CTGCCTGTGG 2100 GGCTGGGGAA AGAAGGAAGA AGAGACACTG GTTAGGTAGG ACTTTTCTAG GTGGAGGGAA 2160 GATGGAGAAG AGTACTTAGA CAAAAGGAAG GATGTGTGTG CAGGAAGCTC CCAAGAACGG 2220 TATGCATACG GTGTATTGGG GAACCTCGTG TAGCTTCATG TCACTTTCCT TCCCTCTCCC 2280 GTTGTTGCTG TCACCCTGTT CGTAGAAAGT GAGTGCTCTT TCCTCAAAGA TTCCCCTCAG 2340 CTCACATGGG GACAGGTATT TTTGGAGCCC CTGGCTGGCA TGAAGCATGG GTCTGCAATG 2400 GTAGATCCAT GTTTGCCAGC CTGGGGACTC CCACACCACT ATCCTGAGAC TGACCCCTGG 2460 GCCATGATTT 2470
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