Variant report

Variant	rs1734936
Chromosome Location	chr21:41488565-41488566
allele	A/G
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]
rs2837429	0.96[EUR][1000 genomes]
rs2837436	0.90[EUR][1000 genomes]
rs2837438	0.90[CEU][hapmap];0.90[EUR][1000 genomes]
rs34869212	0.95[EUR][1000 genomes]
rs402435	0.90[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.90[YRI][hapmap];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs449998	0.81[AMR][1000 genomes]
rs7280514	0.95[EUR][1000 genomes]
rs7280922	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs8134334	0.84[ASN][1000 genomes]
rs9978453	0.90[CEU][hapmap];0.90[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:41487600-41488600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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