| Tag | Content |
|---|
EnhancerAtlas ID | HS062-09920 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr2:241790500-241791430 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr2:241790893-241790908 | TGACCTCTGACCCCA | - | 7.91 | | Nr2f6 | MA0677.1 | chr2:241790893-241790907 | TGACCTCTGACCCC | - | 7.03 | | Rxra | MA0512.2 | chr2:241790893-241790907 | TGACCTCTGACCCC | - | 6.98 | | Zfx | MA0146.2 | chr2:241790605-241790619 | CAGGCCCAGGCGGG | - | 6.37 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 241790525 | 241791266 | | chr2 | 241791304 | 241791424 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I240851 | chr2 | 241790721 | 241790890 |
|
Enhancer Sequence | GCCCCATGGA CTGTGCTGCA GGTGGCCACT GTCACGTCAC CCAGGCCAAG CACACCCGTC 60
AGGATTCCCA AGGCAGGTCG GTGTCCAGCC GCTTCCCTGA GGCTGCAGGC CCAGGCGGGC 120
TGCGGAGTCT GTGCCTACAT ACCGCGGGCC GAGCTTGCTC CAGGCAGGGA CGGCGCGGGA 180
GGCACAGGTC CTCTTTGGGC CTTTCTGCAG GTCCTCCTGC CCCACATGGA CATGCCAGCT 240
GTCACTTGCA CCATCAGGAA GAACAAGAAT CCTGTGTGCC CTGTGGTGGG GCCACAGTCG 300
GCCGCTAGGT GTCACTGTTT CCTCAGAGAC CAGCACATTG TCCCTATGCT TTCTCTCTGC 360
AGTCCCTGGC TGGCAGCTCC TTGGGCAGGG TGGTGACCTC TGACCCCAGA CCCGTCCCCC 420
CTGAGCTGGT CCTGGCTCCA CCGGGAGCTC CGTCCCCTGG GCTTCCTGCT GATATGTAAG 480
TCAAGCCTGA GCTGCCGCGT TGGGGCCACT GATCTGGGCA GAGCCTCGTG GGGTCTCCCA 540
GGGGCTCAGA CGTTGGCCAG GACCCCACAG GGAGGATGCT CAGGTCAAAA AGATGCCCGC 600
ACTCCGGGCG CTGCCCAGAG CTCTTAACTC TCATGCTGAG AACAGCTTTG TGTGCTGAGT 660
GTTTCGCACA CCCGCAGGCC CCGCACGTTC TGCCTGCTGT TCCCTGTAAT CCTGACCTCG 720
CCTGGGAGTG GCAGGGCCAC CCACTTCGGG AGCGGTGGAG ATTGGACTAT TTAGAGCACA 780
CACGCTGGGG AACCAGGGGA AGAGTTGTGA AGGGGTTAAG CAAAAGAAGC CTTTCTCCTG 840
GGCTTGTAGA TGGCCGTCTT CTCCCTGTGT TTCCACATGG CTGCCCCCCA TGTCTGTGTC 900
CTAATCCCCT CTACTTATTA AGACACAGTG 930
|
