Variant report

Variant	rs1157364
Chromosome Location	chr13:70028824-70028825
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1330533	1.00[ASN][1000 genomes]
rs2497365	0.83[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.81[GIH][hapmap];0.82[JPT][hapmap];0.84[ASN][1000 genomes]
rs2593500	0.84[CHD][hapmap]
rs2991962	0.99[ASN][1000 genomes]
rs352250	1.00[ASN][1000 genomes]
rs352255	1.00[ASN][1000 genomes]
rs563789	1.00[ASN][1000 genomes]
rs7329218	0.81[ASN][1000 genomes]
rs9572163	0.87[CHB][hapmap];0.91[CHD][hapmap];0.81[GIH][hapmap];0.82[JPT][hapmap]
rs9634955	0.97[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:70024800-70032000	Weak transcription	Cortex derived primary cultured neurospheres	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