Variant report

Variant	rs2953929
Chromosome Location	chr8:34150505-34150506
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs2168962	0.96[ASN][1000 genomes]
rs2590469	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2609620	0.97[ASN][1000 genomes]
rs2609633	0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2719320	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2719321	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2719322	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28404543	0.92[ASN][1000 genomes]
rs2953926	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2953934	0.99[ASN][1000 genomes]
rs2953935	0.99[ASN][1000 genomes]
rs2959323	0.99[ASN][1000 genomes]
rs2959325	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2978837	1.00[ASN][1000 genomes]
rs4739544	0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6987252	0.99[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:34149200-34152600	Weak transcription	Fetal Brain Male	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