Tag | Content |
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EnhancerAtlas ID | HS098-26636 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr18:77348600-77351070 |
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 | GGTCTCCACT GTGCTTATTT AGAGCAGAGC ACAACTCTCC TTGCGTCTGA GTCCCTTCAC 60 ACAGGTGACT GAGAGGCTCA GGACAGAGCA TTGCAGGGGA GACAGAGGAG GGGCTCGGCC 120 TCGCCAAGCA GCTGGCTCTA TTCATTTAGC AGAACCGCTG CCCCACCCCC TCCCAGCCCC 180 TGCACGGAGG GAGGCCACTG GGGCCGGCCC GTCCCCAACT TCTATTTTGT TTTCGCCAGA 240 GCCGCCTCCA GACTCCCTCT TCACATTTTA TGTCAACTCT GGGGCCCTGC TGGCTGAAAG 300 TGAGTTCTGT TTTCCGGCAG CCCTGTGGCT TTTGGACTCG GCCTTGAAAT TAGTTCATGG 360 CGACCCAGGC ACACATCGCG CTGGGAAGCC ACGTGGGAGC CGTGCGGGTG GAGCGGCCGC 420 CACAGCCAGA CTGAAATGTA GCACAGCGCC TGGGCCTCGT CAGGCCTTTA TGACAGAGTG 480 TAAAGGGAAT TGCTGCTTAG TCACCAATTT GCTTGGCAAG ATTGGATGGA TTAGGAAACA 540 CGTCGAAGGT CAGACAGTAG GAGTTTGTCT AGACGCTCTA TTTTGGACTC GGCGCTGACC 600 CGAGGTGTTT CTGTAGCAAC CTTTACAACA CTGCTATTCT GGCAATATTG GAGAAAACAT 660 GATCCCTCCC ATCATCAGGT AGGGCCCGCT CTGAAAATCC TCGCCCCATC GCTGGGTTTG 720 CTGAGGCGCC TCCAACTCCA TTTAGGACGA GGAAGCCCGA CGGGGAGGCC CCTGGGAGGG 780 ACCGGCTGCT TGGGCGGAGG CCAGGCCTCG GGAAGCTTGT CCAAGGCTCA CAGGGAAAAG 840 CGCCAAGAAA TGGAAGTGGC TCATTTTTCC TCTGGGCCTG AGGGGAAGGT TTTGATTTTA 900 CAGCCGCCCC TAGTCATTTC TCACAGGTTT GAAGCAGACC TTTCCAGGGA CGGGGGAGGG 960 AGAAGGGAGA TGGGGAAGGA TGGGGAGACG CCGTGAGGAG GCAGCCACCT CCGGGGATCC 1020 CCGGAAGCCT GGACGTGCTC TGCCCGGTGG TTCTGTCCCC AGGGAACACG TGGTCATGTC 1080 TGGAGGCATC TGTGGCTGTC ACAGTCATGG TATGGGGTGC TCCTGGCATA GAGGGGTGGG 1140 GCTGCTTCCT TTTGCCTGTC CCTGCTGCCC TCCCCGCCCT CCATGTCTCC CTGCCACCTG 1200 CCCTGCCCTC CCCACCCTGC ATGTCTCACT CTCCATCGTA CCTGAGGGCC CTCTGCCAGC 1260 TGGGAGAGGG GACAGCCCAG GCTTCAGTTT CCCTGCATTT CCCCGGGAGT AGGGGAGCCA 1320 CGAGCAGTCC GTAGGTTCCC TCTTCCTCCC AGGGCCTCAG CACCAGATCC TGGAGCTCCG 1380 GACCCCGCAG TGGGTTCCCC AGCCTCACAG CCCTCCTGGG GCCCCACAGG GGAGGGACGC 1440 AAAGCTGGCT CTGCAGCTCC TTAGCGCGTG ACCTCTGGCA ACTTCAGCCT CTCCTGCCTC 1500 AGTTTCCCGA ACTCTGAAGG GAGGGCGAGT GACACGATGA TTCCTCAGCA GAGACCCCAG 1560 GCCTCTCTCT CCCACTGACC GCCCAGGGGA GTGAAAGTCC AGGACTCCGT GCATGCCTGG 1620 GGACCCGGGC AGTGGGGGAG CAGAACCGGG GACCCGGGCA GCGGGGGAGC AGAACTGCAG 1680 GCCCGGCCGC AGCACCTGCC CACCTTGCTG GTGAGGGGTG AAGGCTTCCA GGCCCTGGCC 1740 TCCACATCCA GACACCACCC TCACCCGTGC AGGAGCGGGA CTCGAACCCA CCTCTCTCGC 1800 CTCCTTGTGC TGCAGGGAAC ATTCAAGTCC TGATGTGGAC TCTGTCCTGC TGCAGCAGGA 1860 AATCCAGAGA TGCCTCTGCC ACCACGGCAA CGGGCTCTGG CCAGAGCAGC AGGAGGGAGC 1920 TGGGCCCACA TGGCCGTCAC CGTGGTTTGC CCACAGCTGC TGTTTCTGAG CCGTCACAGG 1980 GTCAGGGGCA TCCAGGGAAC ACGCTGAGAT GCAGCCTCTG CTGCAGCCCG ACAGATGTGT 2040 AGCTGCTTCT GGAGCACGCC CGGGGAACAC CCTTTCTTCC TATGGATGCC AGCTGGACTC 2100 ACTGTGCAGA CAGGGCCTGA ACCAGACCAG AGGCACTGGC TTCTAGGCGA GGGACCTTCT 2160 CAGCACGGGA CCTGCAGCTG CCTTTCCCAC ACTCACACAG GCTCTTCCCA TTGTCCTAAG 2220 AACCCTGTGG AGGTACAGGC AGGGGTTATC CAAATGCTGA CTCATGTGAG TCCGACAGGA 2280 GCATGGTGCC CGCCCGAGGA GTGTCGACCT CACGCTAGCC ACTGTGATTA TTGTCACTGT 2340 TACTGTGTGA GCTGCTCTGT TCGGGAGGGG AAGCCACGCT GAGGAGCAGC TGGGACACGT 2400 GCCTGGCCCT GCCCTCCAGC TGGCCTCCGT TCCACACATG AGAGCCTTGC CTAGAAGGCC 2460 CTTGGTGGTG 2470
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