Tag | Content |
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EnhancerAtlas ID | HS187-15167 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr20:31329600-31331110 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr20:31330711-31330731 | CCCCAAAACTCCCCACGCCC | + | 6.27 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCACATGCTG TATAGGTTTG TAGCCTAGGA GCAATGCGCT ATACCATATA TCCTAGGGTG 60 CAGTAGGTTT GTGTAAATAA ACTCTAGGAT GCTTGCATAA GATGAACTCA GGGCTGGGCA 120 CAGTGGCTCA CGCCTGTAAT CCCAACACTC TGGGAGGCTG AGGTGGGCAG ATCACCTGAG 180 GTCAGGTGTT CAAGACCAGC CTGGCCAACA TGGTCAAACC CCATCTCTAC TAAAAATACA 240 AAAATTAGCT GGGCATGGTG GCGTGTGCCT GTAGTCCCAG TTACTCGGGA GACTGAGACA 300 GAGAACTGGT TGAACCTGGG AGGCGGAGGT TGCAGTGACC CGAGATCGCG CCACTGCACT 360 CCAGCCTGGG TGACAGAATG AGACTACGTC TCAAAAAAAA AAAATTAATT TCCATTTCTA 420 TTTAATTTTT AAATGTGGCT ACTACAAAAT GCAAAGTTAG AAATGTGGCT TGCAAATTTT 480 TCTATTGCAT AGCTCAAGCT TAGAACCTTC CTGTCGTTAC AAGTTCTAAG TTTGGTTTTT 540 ATCTCGCAAG CAGCACTACT GTGTGGGAAG TTGTGGGGGG TATGGAGATG AAAGAAGAGG 600 GGCGCTACCT CCTGGGAAGT GACAACCTAG CGGGGGAAAT AGATGTATCT TCCCAGTGGG 660 GGTGAGAAGT GTCATTCTCA CCTATTTCAG CAGCCTTGGT GGTATGAAAA GGCATCCCAA 720 CCAGCACAGA AGCAGGATGC CTCCAAGACT GCCTTGGTTG GCACCTGCAG CCTGAAGGGG 780 GAGAAAAAGG CTTTGCTAGC TCCCCTACCA TCGAGGATGA AGACCCCCAC TGTACACAGT 840 GTATAAGGTT TCTTTCCATG TGAATCCCAG TGACTCTCCT TAACTGGGTG GAGGTGGAAG 900 GTGTCATCAG CCTTGTCCCA GATCGAGCCC CTCAGGCCCA CAGAGCCCCA GTGGGGCCTG 960 GCTATTACTG ACACTCATGT CACACTGAGA TGTAAGACGG CAGCCCAGGC CAAGCTTCCC 1020 CGGGCCCCCT CAGATTCTCG GGCCCTCCCA CTCCCCTCAG GCTTCCTCGG CCTCCCTGCC 1080 AAACATCTAT CTCCCTTTGG ACCCCACTGC TCCCCAAAAC TCCCCACGCC CTTAGTCTGT 1140 TCCTTCAGTT CCCCAAACTC CTTCAGCCTC ATCTAGACTC CCCTCCGTCC CTCTTCTAGG 1200 ACCCCAAAAG CTCTCCTCGG CCCCAGGACC CCGCAGAGGT CCCGTAGTCC CATCTCTGAG 1260 ACCCCACAAA GCCTTTCGGA CCCCTCAGGT GGCCCTTAGG CCTCCGGAGA TCCCTTGGCT 1320 CCCCACACTC TCCTCAGACC CCAGCTCACC TTAGCCTCGC CCCGAACCCA CCTCACACAC 1380 CCCAAACGCC CACAAGACGC CGCTCTGTCT AGTCTCTCCC AACTCCCGCG CACCCCCGGA 1440 CGTCCCCCCC ACCCCAGGCC CGGATCCTGG AATCACCTGG GCCCCGCGCC CCACGCCCCG 1500 CCGCCGGGCC 1510
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