Variant report

Variant	rs11777613
Chromosome Location	chr8:79007681-79007682
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11775863	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11784367	0.81[EUR][1000 genomes]
rs12677810	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12680674	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13248802	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs16939614	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs16939622	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs35370736	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6989014	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7010818	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9298308	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:78997000-79010000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr8:79006400-79008200	Enhancers	Fetal Brain Female	brain
3	chr8:79006400-79008600	Enhancers	Brain Germinal Matrix	brain

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links