Variant report

Variant	rs11927030
Chromosome Location	chr3:50789602-50789603
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]
rs11914934	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs11915036	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs62257803	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs62257807	1.00[AFR][1000 genomes]
rs62257814	1.00[AFR][1000 genomes]
rs62258667	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs62258672	0.81[EUR][1000 genomes]
rs62260125	1.00[AFR][1000 genomes]
rs62260128	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs62260156	1.00[AFR][1000 genomes]
rs62263011	1.00[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50776000-50790000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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