| Tag | Content |
|---|
EnhancerAtlas ID | HS165-08819 | Organism | Homo sapiens | Tissue/cell | Ramos | Coordinate | chr20:31329870-31331110 | 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 | GTAGTCCCAG TTACTCGGGA GACTGAGACA GAGAACTGGT TGAACCTGGG AGGCGGAGGT 60
TGCAGTGACC CGAGATCGCG CCACTGCACT CCAGCCTGGG TGACAGAATG AGACTACGTC 120
TCAAAAAAAA AAAATTAATT TCCATTTCTA TTTAATTTTT AAATGTGGCT ACTACAAAAT 180
GCAAAGTTAG AAATGTGGCT TGCAAATTTT TCTATTGCAT AGCTCAAGCT TAGAACCTTC 240
CTGTCGTTAC AAGTTCTAAG TTTGGTTTTT ATCTCGCAAG CAGCACTACT GTGTGGGAAG 300
TTGTGGGGGG TATGGAGATG AAAGAAGAGG GGCGCTACCT CCTGGGAAGT GACAACCTAG 360
CGGGGGAAAT AGATGTATCT TCCCAGTGGG GGTGAGAAGT GTCATTCTCA CCTATTTCAG 420
CAGCCTTGGT GGTATGAAAA GGCATCCCAA CCAGCACAGA AGCAGGATGC CTCCAAGACT 480
GCCTTGGTTG GCACCTGCAG CCTGAAGGGG GAGAAAAAGG CTTTGCTAGC TCCCCTACCA 540
TCGAGGATGA AGACCCCCAC TGTACACAGT GTATAAGGTT TCTTTCCATG TGAATCCCAG 600
TGACTCTCCT TAACTGGGTG GAGGTGGAAG GTGTCATCAG CCTTGTCCCA GATCGAGCCC 660
CTCAGGCCCA CAGAGCCCCA GTGGGGCCTG GCTATTACTG ACACTCATGT CACACTGAGA 720
TGTAAGACGG CAGCCCAGGC CAAGCTTCCC CGGGCCCCCT CAGATTCTCG GGCCCTCCCA 780
CTCCCCTCAG GCTTCCTCGG CCTCCCTGCC AAACATCTAT CTCCCTTTGG ACCCCACTGC 840
TCCCCAAAAC TCCCCACGCC CTTAGTCTGT TCCTTCAGTT CCCCAAACTC CTTCAGCCTC 900
ATCTAGACTC CCCTCCGTCC CTCTTCTAGG ACCCCAAAAG CTCTCCTCGG CCCCAGGACC 960
CCGCAGAGGT CCCGTAGTCC CATCTCTGAG ACCCCACAAA GCCTTTCGGA CCCCTCAGGT 1020
GGCCCTTAGG CCTCCGGAGA TCCCTTGGCT CCCCACACTC TCCTCAGACC CCAGCTCACC 1080
TTAGCCTCGC CCCGAACCCA CCTCACACAC CCCAAACGCC CACAAGACGC CGCTCTGTCT 1140
AGTCTCTCCC AACTCCCGCG CACCCCCGGA CGTCCCCCCC ACCCCAGGCC CGGATCCTGG 1200
AATCACCTGG GCCCCGCGCC CCACGCCCCG CCGCCGGGCC 1240
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