Variant report

Variant	rs9493540
Chromosome Location	chr6:133480179-133480180
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10457600	0.84[EUR][1000 genomes]
rs10457602	0.95[CEU][hapmap]
rs10457603	0.95[CEU][hapmap]
rs11154715	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12154207	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12190728	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12191026	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12196069	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12196492	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12199138	0.84[EUR][1000 genomes]
rs12199555	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12199738	0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12199958	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12200393	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12201315	0.95[CEU][hapmap]
rs12206291	0.81[EUR][1000 genomes]
rs12210216	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12211999	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12213350	0.84[EUR][1000 genomes]
rs12213452	0.84[EUR][1000 genomes]
rs12213690	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12215217	0.84[EUR][1000 genomes]
rs1856291	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs59793266	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs62428563	0.83[EUR][1000 genomes]
rs62428596	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs62428597	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6913444	0.86[EUR][1000 genomes]
rs7746390	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7748926	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7750218	0.86[EUR][1000 genomes]
rs7750279	0.95[CEU][hapmap];0.86[EUR][1000 genomes]
rs7750376	0.95[CEU][hapmap];0.86[EUR][1000 genomes]
rs7754486	0.95[CEU][hapmap];0.83[EUR][1000 genomes]
rs7756171	0.90[CEU][hapmap]
rs7756963	0.87[EUR][1000 genomes]
rs7766470	0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7767378	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7767651	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7770031	0.86[EUR][1000 genomes]
rs7773069	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9483554	0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9483557	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9493544	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs957183	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428154	chr6:133271975-133522803	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	esv2758080	chr6:133444719-133627364	Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv2759470	chr6:133444719-133627364	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv886677	chr6:133454738-133515602	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9493540	TAAR2	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133480000-133480800	Enhancers	Cortex derived primary cultured neurospheres	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links