Variant report

Variant	rs35629779
Chromosome Location	chr10:95623661-95623662
allele	A/G
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]
rs10786145	0.95[ASN][1000 genomes]
rs10882355	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10882356	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10882362	0.95[ASN][1000 genomes]
rs11187680	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11187721	1.00[ASN][1000 genomes]
rs11187722	1.00[ASN][1000 genomes]
rs11187723	1.00[ASN][1000 genomes]
rs11187728	0.95[ASN][1000 genomes]
rs12356200	0.95[ASN][1000 genomes]
rs12413002	0.95[ASN][1000 genomes]
rs2113955	0.95[ASN][1000 genomes]
rs34424393	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4919616	0.95[ASN][1000 genomes]
rs7068140	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7096071	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:95619600-95630000	Weak transcription	Fetal Intestine Large	intestine

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