Variant report

Variant	rs16939605
Chromosome Location	chr8:79005815-79005816
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10957883	0.90[EUR][1000 genomes]
rs16939604	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16939611	0.96[EUR][1000 genomes]
rs16939613	0.93[EUR][1000 genomes]
rs16939626	0.84[EUR][1000 genomes]
rs2128019	0.83[EUR][1000 genomes]
rs56080040	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62510273	1.00[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs62510274	1.00[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs6995312	0.89[EUR][1000 genomes]
rs6997505	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72674515	0.94[EUR][1000 genomes]

No data

Chromatin state (count:1 , 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

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