| Tag | Content |
|---|
EnhancerAtlas ID | HS121-13187 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr16:782370-783290 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr16:782994-783005 | GGTGACTCATG | + | 6.62 | | FOSL2 | MA0478.1 | chr16:782993-783004 | GGGTGACTCAT | + | 6.14 | | JUNB | MA0490.1 | chr16:782993-783004 | GGGTGACTCAT | + | 6.32 | | JUND | MA0491.1 | chr16:782994-783005 | GGTGACTCATG | + | 6.02 | | NR2C2 | MA0504.1 | chr16:782714-782729 | CGACCTCTGCCCCCC | - | 6.45 | | Nr2f6(var.2) | MA0728.1 | chr16:782856-782871 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CTCCTGCAAA GAAGCCACAG CGCAGACACT CTTTAGCGGA GATCCCAGCA ACAAAGTCAG 60
AGAACATCCA AGCCACCTGC ATCCCCAGCA GTCTGCACTT TGGCCCCAGA AGGCCCCAAA 120
TGTCCACCCT AGCCCGTGGT GGGGAGGCCA GGCCCGGTCA CTCCTGAAGC CCCTCTGGAG 180
GCTGCCTGGT CCTGCCCAGG GAGGTGTGCC AGCGGCCAGG CCACTCTGCT CACCCAGTGT 240
CCATCTGTCC ATCCTCTTAG GCAGTCTGCT TTTCTTTTTT TTTTGAGACG GAGTCTCACT 300
CTGCCGCCCA GGCTGGAGTG CAATGGTACG ATCTCGGCTC ACTACGACCT CTGCCCCCCG 360
GGATCAAGTG ACTCTCCTGC CTCAGCCTCC CGAGTAGCTG GGATTACAGG AGCACCACCA 420
CTACTCCCGG CTAATTTTCG TATTTTTAGT AGACATGGGG TTTCATCATC TCGGCCAGGC 480
TGGTCTTGAA CTCCTGACCT CGTGATCCAC CCACCTCTGC CTCCCAAAGT GCTGGGATTA 540
CAGGCGTGAG CCACCATGCC CGGCCACAGT TTGCTTTTCT GCCTCACATT TGGGAGACTG 600
TGGGGCTGCT CGACTCAGGA ATGGGGTGAC TCATGGGAGC TGAAGAGGCT GCATTCGAGA 660
ATCTCTGCCC ACCTCCAAAG ACTCATTTCA GAGCCAACAA GGAGGTATTA CTGAGCGCCA 720
CCTGGCTGCA GGTCCCCAAG ACAGGCCAGC TGCAAATGGG CCCACCTGGC TCCAAGGGGA 780
GAGACGAAGG TACGTGCACG CATGCGAGCC CCCACACTCC AGCCAGGGCC CCCACAGGCA 840
GGATCCTGGG CAGTCGCCAC CTGTGCCCAG GGCTCAGGAA TCAGACCAGG AGGCTTGAGG 900
GCTCAGGGCC GCACGGCGTG 920
|
