Variant report

Variant	rs12123610
Chromosome Location	chr1:56312992-56312993
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10493183	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10493185	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10493187	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10493189	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10493190	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10493191	1.00[ASN][1000 genomes]
rs10888940	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10888942	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10888947	1.00[ASN][1000 genomes]
rs10888948	1.00[ASN][1000 genomes]
rs11206673	0.84[AFR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11206677	0.84[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11206680	1.00[ASN][1000 genomes]
rs11206681	1.00[ASN][1000 genomes]
rs11206689	1.00[ASN][1000 genomes]
rs11206690	1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs11582662	1.00[ASN][1000 genomes]
rs12058087	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12070494	1.00[ASN][1000 genomes]
rs12092701	1.00[ASN][1000 genomes]
rs12118218	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12119904	0.84[AFR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12120132	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12123418	1.00[ASN][1000 genomes]
rs12124871	1.00[ASN][1000 genomes]
rs12138137	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12141873	1.00[ASN][1000 genomes]
rs12145137	1.00[ASN][1000 genomes]
rs17112888	1.00[ASN][1000 genomes]
rs17113073	1.00[ASN][1000 genomes]
rs2067637	1.00[ASN][1000 genomes]
rs41285922	1.00[ASN][1000 genomes]
rs55693755	1.00[ASN][1000 genomes]
rs58538058	1.00[ASN][1000 genomes]
rs59959484	1.00[ASN][1000 genomes]
rs61774839	0.84[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61774843	1.00[ASN][1000 genomes]
rs61777585	1.00[ASN][1000 genomes]
rs61777621	1.00[ASN][1000 genomes]
rs6659096	1.00[ASN][1000 genomes]
rs6662998	1.00[CHD][hapmap]
rs6691673	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7516605	1.00[ASN][1000 genomes]
rs7517205	1.00[ASN][1000 genomes]
rs7517995	1.00[ASN][1000 genomes]
rs7530878	1.00[ASN][1000 genomes]
rs7540772	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829926	chr1:56188492-56360745	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	n/a

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs12123610	ZYG11A	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:56295200-56320400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr1:56310400-56321200	Weak transcription	Psoas Muscle	Psoas

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links