Tag | Content |
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EnhancerAtlas ID | HS105-38180 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr18:77348530-77351020 |
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) |
HEY2 | MA0649.1 | chr18:77350993-77351003 | GACACGTGCC | + | 6.02 | NFE2L1 | MA0089.2 | chr18:77350852-77350867 | AATGCTGACTCATGT | - | 6.29 | NR2F1 | MA0017.2 | chr18:77350064-77350077 | CGCGTGACCTCTG | - | 6.08 | Npas2 | MA0626.1 | chr18:77350993-77351003 | GACACGTGCC | - | 6.02 | ZNF263 | MA0528.1 | chr18:77349555-77349576 | GAGGGAGAAGGGAGATGGGGA | + | 6.49 | ZNF263 | MA0528.1 | chr18:77349558-77349579 | GGAGAAGGGAGATGGGGAAGG | + | 6.91 |
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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 |
GH18I079587 | chr18 | 77347403 | 77350904 |
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Enhancer Sequence | AGCCCAAGTG CCCGAAACCC AGAGCCTCGG ACTCAGGGCA AAAGGAAGCC GCCCCATTCC 60 ACCACATCAG GGTCTCCACT GTGCTTATTT AGAGCAGAGC ACAACTCTCC TTGCGTCTGA 120 GTCCCTTCAC ACAGGTGACT GAGAGGCTCA GGACAGAGCA TTGCAGGGGA GACAGAGGAG 180 GGGCTCGGCC TCGCCAAGCA GCTGGCTCTA TTCATTTAGC AGAACCGCTG CCCCACCCCC 240 TCCCAGCCCC TGCACGGAGG GAGGCCACTG GGGCCGGCCC GTCCCCAACT TCTATTTTGT 300 TTTCGCCAGA GCCGCCTCCA GACTCCCTCT TCACATTTTA TGTCAACTCT GGGGCCCTGC 360 TGGCTGAAAG TGAGTTCTGT TTTCCGGCAG CCCTGTGGCT TTTGGACTCG GCCTTGAAAT 420 TAGTTCATGG CGACCCAGGC ACACATCGCG CTGGGAAGCC ACGTGGGAGC CGTGCGGGTG 480 GAGCGGCCGC CACAGCCAGA CTGAAATGTA GCACAGCGCC TGGGCCTCGT CAGGCCTTTA 540 TGACAGAGTG TAAAGGGAAT TGCTGCTTAG TCACCAATTT GCTTGGCAAG ATTGGATGGA 600 TTAGGAAACA CGTCGAAGGT CAGACAGTAG GAGTTTGTCT AGACGCTCTA TTTTGGACTC 660 GGCGCTGACC CGAGGTGTTT CTGTAGCAAC CTTTACAACA CTGCTATTCT GGCAATATTG 720 GAGAAAACAT GATCCCTCCC ATCATCAGGT AGGGCCCGCT CTGAAAATCC TCGCCCCATC 780 GCTGGGTTTG CTGAGGCGCC TCCAACTCCA TTTAGGACGA GGAAGCCCGA CGGGGAGGCC 840 CCTGGGAGGG ACCGGCTGCT TGGGCGGAGG CCAGGCCTCG GGAAGCTTGT CCAAGGCTCA 900 CAGGGAAAAG CGCCAAGAAA TGGAAGTGGC TCATTTTTCC TCTGGGCCTG AGGGGAAGGT 960 TTTGATTTTA CAGCCGCCCC TAGTCATTTC TCACAGGTTT GAAGCAGACC TTTCCAGGGA 1020 CGGGGGAGGG AGAAGGGAGA TGGGGAAGGA TGGGGAGACG CCGTGAGGAG GCAGCCACCT 1080 CCGGGGATCC CCGGAAGCCT GGACGTGCTC TGCCCGGTGG TTCTGTCCCC AGGGAACACG 1140 TGGTCATGTC TGGAGGCATC TGTGGCTGTC ACAGTCATGG TATGGGGTGC TCCTGGCATA 1200 GAGGGGTGGG GCTGCTTCCT TTTGCCTGTC CCTGCTGCCC TCCCCGCCCT CCATGTCTCC 1260 CTGCCACCTG CCCTGCCCTC CCCACCCTGC ATGTCTCACT CTCCATCGTA CCTGAGGGCC 1320 CTCTGCCAGC TGGGAGAGGG GACAGCCCAG GCTTCAGTTT CCCTGCATTT CCCCGGGAGT 1380 AGGGGAGCCA CGAGCAGTCC GTAGGTTCCC TCTTCCTCCC AGGGCCTCAG CACCAGATCC 1440 TGGAGCTCCG GACCCCGCAG TGGGTTCCCC AGCCTCACAG CCCTCCTGGG GCCCCACAGG 1500 GGAGGGACGC AAAGCTGGCT CTGCAGCTCC TTAGCGCGTG ACCTCTGGCA ACTTCAGCCT 1560 CTCCTGCCTC AGTTTCCCGA ACTCTGAAGG GAGGGCGAGT GACACGATGA TTCCTCAGCA 1620 GAGACCCCAG GCCTCTCTCT CCCACTGACC GCCCAGGGGA GTGAAAGTCC AGGACTCCGT 1680 GCATGCCTGG GGACCCGGGC AGTGGGGGAG CAGAACCGGG GACCCGGGCA GCGGGGGAGC 1740 AGAACTGCAG GCCCGGCCGC AGCACCTGCC CACCTTGCTG GTGAGGGGTG AAGGCTTCCA 1800 GGCCCTGGCC TCCACATCCA GACACCACCC TCACCCGTGC AGGAGCGGGA CTCGAACCCA 1860 CCTCTCTCGC CTCCTTGTGC TGCAGGGAAC ATTCAAGTCC TGATGTGGAC TCTGTCCTGC 1920 TGCAGCAGGA AATCCAGAGA TGCCTCTGCC ACCACGGCAA CGGGCTCTGG CCAGAGCAGC 1980 AGGAGGGAGC TGGGCCCACA TGGCCGTCAC CGTGGTTTGC CCACAGCTGC TGTTTCTGAG 2040 CCGTCACAGG GTCAGGGGCA TCCAGGGAAC ACGCTGAGAT GCAGCCTCTG CTGCAGCCCG 2100 ACAGATGTGT AGCTGCTTCT GGAGCACGCC CGGGGAACAC CCTTTCTTCC TATGGATGCC 2160 AGCTGGACTC ACTGTGCAGA CAGGGCCTGA ACCAGACCAG AGGCACTGGC TTCTAGGCGA 2220 GGGACCTTCT CAGCACGGGA CCTGCAGCTG CCTTTCCCAC ACTCACACAG GCTCTTCCCA 2280 TTGTCCTAAG AACCCTGTGG AGGTACAGGC AGGGGTTATC CAAATGCTGA CTCATGTGAG 2340 TCCGACAGGA GCATGGTGCC CGCCCGAGGA GTGTCGACCT CACGCTAGCC ACTGTGATTA 2400 TTGTCACTGT TACTGTGTGA GCTGCTCTGT TCGGGAGGGG AAGCCACGCT GAGGAGCAGC 2460 TGGGACACGT GCCTGGCCCT GCCCTCCAGC 2490
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