| Tag | Content |
|---|
EnhancerAtlas ID | HS098-09455 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr11:18105460-18106600 | 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 | TATTTCAGGT TTTGGTTAAG TTCTATGAAG GAAATAAAAG AGGAATATAA TATAGCAGCC 60
TAGCAGGGCT AGCTCTCTGA CAAGGTAACA TTGAGTTGAG AACTAAAGCA ATGAAGCATC 120
AGCAATTAAA ATACCCTAGG AGGTCAGGGG TGGTAGCTCA CGCTTGTAAT CTGAGCAGTT 180
TGAGAGGCCA AGATGGGCGG GTAGCTTGAG CCCAGGAGTT CGAGACCAGC CTGAGCAATA 240
TGGTGAAACC GTGTCTTTAC AAAAAGTACA AAAAAATTAG CTCACAGGAT TTTTCTACCA 300
CTACCACTGT TACCATCTTG GTCCAAGTTA TAACATTTCT TGCTATGAGT CAATTATGAA 360
GAATCTCTAA AAGCCTCCTA ACTCATGTCC CTTTTGTACC CATGACTCCC CATATTTCTC 420
ATCAAAACAG CAGCCTATTA AAGCCAGCTC ATGCGTAGGC AACTTCTGCT TAAAACCCAC 480
CATGGTTCCC CACCTCATTC AGAGGAAAAG GCAACATCAG GCCCTCCATA CTCTACCTCT 540
CTGGCTCCAT GTGCTACTTT GCTAAATCCA CCCCAGCCAT ATGGGATCTC ACTGTTCCTC 600
CTCAAAGACA CCAGGCATAC TTCTGGTTGA AGGCTTTTAC ACTTTCCATT CCCTCTGTCT 660
GGAATGTTCT TCTCCCCAAG TATGCACATG ACTCCCTCCA TTCTGTCCCT AAGGACTGTA 720
CTCAATGCCA CCTTCTCAAT GAGGTAACGT ATCTACAAAT GAAGATCTTA AAAATATTCA 780
ACATTCCTTT TTTATTAAAA ACTCTTAATA AAATAGAAAC AGATTAATAT TTCCTTAAAT 840
GGTAAGACAT ATATCTGTTT TTGGAGGGGG GGTGCGGAGT ATTGCTCTGC TGCCCAGGCT 900
GGAGTACAAT GGCGTGATTT CAGCTCACTG CAGCCTCTGC CTCCCAGGTT CGAGCAACTC 960
TCCTGCCTCA GCCTTCTGAG TAACTGAGAT TACAGGCATG CGTCACCAAG CCTGGCTAAT 1020
TTTTGTATTT TTAGCAGAGA CAGGGTTTCA CCATGTTAGC CAGACTGACT TTGAACTCCT 1080
GACCTCAGGT AATCTGCCCG CCTCAGCCTC CCAAAGTGCT GGGATTATAG GTGTGAGCCA 1140
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