Variant report

Variant	rs11013432
Chromosome Location	chr10:23678019-23678020
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]
rs11013427	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11013433	0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56984761	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57142582	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7077959	1.00[EUR][1000 genomes]
rs7078402	1.00[EUR][1000 genomes]
rs7085674	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7101025	1.00[EUR][1000 genomes]
rs73602541	1.00[EUR][1000 genomes]
rs73602543	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73602544	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73602547	1.00[EUR][1000 genomes]
rs73602571	1.00[EUR][1000 genomes]
rs7921695	1.00[EUR][1000 genomes]
rs9651373	1.00[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23671000-23679600	Weak transcription	Placenta	Placenta

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