Tag | Content |
---|
EnhancerAtlas ID | HS042-28100 | Organism | Homo sapiens | Tissue/cell | Fetal_brain | Coordinate | chr20:31329620-31331110 | 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 | TAGCCTAGGA GCAATGCGCT ATACCATATA TCCTAGGGTG CAGTAGGTTT GTGTAAATAA 60 ACTCTAGGAT GCTTGCATAA GATGAACTCA GGGCTGGGCA CAGTGGCTCA CGCCTGTAAT 120 CCCAACACTC TGGGAGGCTG AGGTGGGCAG ATCACCTGAG GTCAGGTGTT CAAGACCAGC 180 CTGGCCAACA TGGTCAAACC CCATCTCTAC TAAAAATACA AAAATTAGCT GGGCATGGTG 240 GCGTGTGCCT GTAGTCCCAG TTACTCGGGA GACTGAGACA GAGAACTGGT TGAACCTGGG 300 AGGCGGAGGT TGCAGTGACC CGAGATCGCG CCACTGCACT CCAGCCTGGG TGACAGAATG 360 AGACTACGTC TCAAAAAAAA AAAATTAATT TCCATTTCTA TTTAATTTTT AAATGTGGCT 420 ACTACAAAAT GCAAAGTTAG AAATGTGGCT TGCAAATTTT TCTATTGCAT AGCTCAAGCT 480 TAGAACCTTC CTGTCGTTAC AAGTTCTAAG TTTGGTTTTT ATCTCGCAAG CAGCACTACT 540 GTGTGGGAAG TTGTGGGGGG TATGGAGATG AAAGAAGAGG GGCGCTACCT CCTGGGAAGT 600 GACAACCTAG CGGGGGAAAT AGATGTATCT TCCCAGTGGG GGTGAGAAGT GTCATTCTCA 660 CCTATTTCAG CAGCCTTGGT GGTATGAAAA GGCATCCCAA CCAGCACAGA AGCAGGATGC 720 CTCCAAGACT GCCTTGGTTG GCACCTGCAG CCTGAAGGGG GAGAAAAAGG CTTTGCTAGC 780 TCCCCTACCA TCGAGGATGA AGACCCCCAC TGTACACAGT GTATAAGGTT TCTTTCCATG 840 TGAATCCCAG TGACTCTCCT TAACTGGGTG GAGGTGGAAG GTGTCATCAG CCTTGTCCCA 900 GATCGAGCCC CTCAGGCCCA CAGAGCCCCA GTGGGGCCTG GCTATTACTG ACACTCATGT 960 CACACTGAGA TGTAAGACGG CAGCCCAGGC CAAGCTTCCC CGGGCCCCCT CAGATTCTCG 1020 GGCCCTCCCA CTCCCCTCAG GCTTCCTCGG CCTCCCTGCC AAACATCTAT CTCCCTTTGG 1080 ACCCCACTGC TCCCCAAAAC TCCCCACGCC CTTAGTCTGT TCCTTCAGTT CCCCAAACTC 1140 CTTCAGCCTC ATCTAGACTC CCCTCCGTCC CTCTTCTAGG ACCCCAAAAG CTCTCCTCGG 1200 CCCCAGGACC CCGCAGAGGT CCCGTAGTCC CATCTCTGAG ACCCCACAAA GCCTTTCGGA 1260 CCCCTCAGGT GGCCCTTAGG CCTCCGGAGA TCCCTTGGCT CCCCACACTC TCCTCAGACC 1320 CCAGCTCACC TTAGCCTCGC CCCGAACCCA CCTCACACAC CCCAAACGCC CACAAGACGC 1380 CGCTCTGTCT AGTCTCTCCC AACTCCCGCG CACCCCCGGA CGTCCCCCCC ACCCCAGGCC 1440 CGGATCCTGG AATCACCTGG GCCCCGCGCC CCACGCCCCG CCGCCGGGCC 1490
|
| |
|
|
|