Variant report

Variant	rs7936832
Chromosome Location	chr11:83498450-83498451
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1155310	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1155313	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12290852	0.87[ASN][1000 genomes]
rs56697477	0.94[ASN][1000 genomes]
rs56836954	0.80[ASN][1000 genomes]
rs60904911	0.80[ASN][1000 genomes]
rs66773965	0.81[ASN][1000 genomes]
rs7116773	0.89[ASN][1000 genomes]
rs7118583	0.94[ASN][1000 genomes]
rs7127293	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7130838	0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs716865	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7931558	0.96[ASN][1000 genomes]
rs7937214	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7943895	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:83495400-83503200	Weak transcription	Liver	Liver
2	chr11:83498200-83506600	Weak transcription	Brain Hippocampus Middle	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