Variant report

Variant	rs950031
Chromosome Location	chr1:71220239-71220240
allele	C/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]
rs10493478	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12048393	0.85[CEU][hapmap];0.90[MEX][hapmap];0.93[TSI][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12127573	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12141116	0.87[CEU][hapmap]
rs1325948	1.00[CHD][hapmap]
rs17541777	1.00[CHD][hapmap]
rs2152126	0.85[CEU][hapmap]
rs2782770	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61778712	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6685675	0.98[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6686947	1.00[CHD][hapmap]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:71218800-71221800	Enhancers	K562	blood

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