| Tag | Content |
|---|
EnhancerAtlas ID | HS019-02659 | Organism | Homo sapiens | Tissue/cell | CD20+ | Coordinate | chr11:18105450-18106830 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr11:18106531-18106546 | TGAACTCCTGACCTC | - | 6.22 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 18105803 | 18105911 | | chr11 | 18106021 | 18106083 |
| Enhancer Sequence | TAAAACAGAC TATTTCAGGT TTTGGTTAAG TTCTATGAAG GAAATAAAAG AGGAATATAA 60
TATAGCAGCC TAGCAGGGCT AGCTCTCTGA CAAGGTAACA TTGAGTTGAG AACTAAAGCA 120
ATGAAGCATC AGCAATTAAA ATACCCTAGG AGGTCAGGGG TGGTAGCTCA CGCTTGTAAT 180
CTGAGCAGTT TGAGAGGCCA AGATGGGCGG GTAGCTTGAG CCCAGGAGTT CGAGACCAGC 240
CTGAGCAATA TGGTGAAACC GTGTCTTTAC AAAAAGTACA AAAAAATTAG CTCACAGGAT 300
TTTTCTACCA CTACCACTGT TACCATCTTG GTCCAAGTTA TAACATTTCT TGCTATGAGT 360
CAATTATGAA GAATCTCTAA AAGCCTCCTA ACTCATGTCC CTTTTGTACC CATGACTCCC 420
CATATTTCTC ATCAAAACAG CAGCCTATTA AAGCCAGCTC ATGCGTAGGC AACTTCTGCT 480
TAAAACCCAC CATGGTTCCC CACCTCATTC AGAGGAAAAG GCAACATCAG GCCCTCCATA 540
CTCTACCTCT CTGGCTCCAT GTGCTACTTT GCTAAATCCA CCCCAGCCAT ATGGGATCTC 600
ACTGTTCCTC CTCAAAGACA CCAGGCATAC TTCTGGTTGA AGGCTTTTAC ACTTTCCATT 660
CCCTCTGTCT GGAATGTTCT TCTCCCCAAG TATGCACATG ACTCCCTCCA TTCTGTCCCT 720
AAGGACTGTA CTCAATGCCA CCTTCTCAAT GAGGTAACGT ATCTACAAAT GAAGATCTTA 780
AAAATATTCA ACATTCCTTT TTTATTAAAA ACTCTTAATA AAATAGAAAC AGATTAATAT 840
TTCCTTAAAT GGTAAGACAT ATATCTGTTT TTGGAGGGGG GGTGCGGAGT ATTGCTCTGC 900
TGCCCAGGCT GGAGTACAAT GGCGTGATTT CAGCTCACTG CAGCCTCTGC CTCCCAGGTT 960
CGAGCAACTC TCCTGCCTCA GCCTTCTGAG TAACTGAGAT TACAGGCATG CGTCACCAAG 1020
CCTGGCTAAT TTTTGTATTT TTAGCAGAGA CAGGGTTTCA CCATGTTAGC CAGACTGACT 1080
TTGAACTCCT GACCTCAGGT AATCTGCCCG CCTCAGCCTC CCAAAGTGCT GGGATTATAG 1140
GTGTGAGCCA CAGCACCTGG CTGTAAAACA TATATCTTAT ACCCAATAAT GCTTAACAAT 1200
GGAACTCTAG GATTATTCCT ACTAAAATCA GGAAGAAGGT AAGGATGTTT TCTACCATCA 1260
CTATTATTTT ACACCAGAGA CTCTAGGCAA CCCAGAAAGA CAAGAAGAAT AAACCAGAGA 1320
TAGACAAGTG ATAAAATATA TCTAACTTAA GCCAAAGCAC TATCAGATAA AGCCCAAAGA 1380
|
| |
|
|
|
