Variant report

Variant	rs9492018
Chromosome Location	chr6:128907604-128907605
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 135 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:132)

rs_ID	r²[population]
rs10085245	1.00[ASN][1000 genomes]
rs10085247	1.00[ASN][1000 genomes]
rs10085248	1.00[ASN][1000 genomes]
rs1012629	1.00[CHD][hapmap]
rs10223535	1.00[ASN][1000 genomes]
rs10872331	1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs11154439	1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs11154440	1.00[CEU][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11751628	1.00[ASN][1000 genomes]
rs11752256	1.00[ASN][1000 genomes]
rs11753496	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11756545	1.00[CHD][hapmap]
rs11758545	1.00[ASN][1000 genomes]
rs11758690	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11963575	1.00[ASN][1000 genomes]
rs12524679	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12525214	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12526634	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12526667	1.00[ASN][1000 genomes]
rs12527086	0.85[CEU][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12527265	1.00[CEU][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12529229	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12529511	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12529947	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12529948	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1341584	1.00[CEU][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1341585	0.86[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1341588	0.81[EUR][1000 genomes]
rs13437323	1.00[ASN][1000 genomes]
rs1417896	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1572964	0.92[CEU][hapmap];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17055952	1.00[ASN][1000 genomes]
rs17056043	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17364020	1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs17364090	1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs17364118	1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs17364153	1.00[ASN][1000 genomes]
rs17460940	1.00[CHD][hapmap]
rs17461290	1.00[CHD][hapmap]
rs17461370	1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs17461759	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs1935131	1.00[ASN][1000 genomes]
rs2144376	1.00[CEU][hapmap]
rs2326702	1.00[ASW][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];0.95[LWK][hapmap];1.00[MKK][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55988836	1.00[ASN][1000 genomes]
rs57922933	1.00[ASN][1000 genomes]
rs62425737	1.00[ASN][1000 genomes]
rs62425738	1.00[ASN][1000 genomes]
rs62425739	1.00[ASN][1000 genomes]
rs62425740	1.00[ASN][1000 genomes]
rs62425742	1.00[ASN][1000 genomes]
rs62425743	1.00[ASN][1000 genomes]
rs62425744	1.00[ASN][1000 genomes]
rs62426790	1.00[ASN][1000 genomes]
rs62426791	1.00[ASN][1000 genomes]
rs62426792	1.00[ASN][1000 genomes]
rs62426793	1.00[ASN][1000 genomes]
rs62426794	1.00[ASN][1000 genomes]
rs62426795	1.00[ASN][1000 genomes]
rs62426796	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426797	1.00[ASN][1000 genomes]
rs62426798	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426799	1.00[ASN][1000 genomes]
rs62426800	1.00[ASN][1000 genomes]
rs62426801	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426804	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426805	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426806	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426840	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426841	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426842	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426844	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426845	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62426846	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426847	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426848	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426849	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426850	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426851	1.00[ASN][1000 genomes]
rs62426853	1.00[ASN][1000 genomes]
rs62427780	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62427781	1.00[ASN][1000 genomes]
rs6569529	1.00[ASN][1000 genomes]
rs6569535	1.00[CEU][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap];0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6569536	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6916294	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs714782	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs717617	0.86[CEU][hapmap]
rs7356818	1.00[ASN][1000 genomes]
rs7356823	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7356912	1.00[ASN][1000 genomes]
rs7454742	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs766306	1.00[ASN][1000 genomes]
rs7738739	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7739600	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7748742	1.00[ASN][1000 genomes]
rs7751094	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7751265	1.00[CEU][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap];0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7752487	1.00[ASN][1000 genomes]
rs7754729	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7760287	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7760572	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7760682	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7765212	1.00[ASN][1000 genomes]
rs7768240	1.00[CEU][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7771701	1.00[ASN][1000 genomes]
rs9321122	1.00[ASN][1000 genomes]
rs9375578	1.00[CEU][hapmap];0.92[TSI][hapmap];0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9388647	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9388648	0.92[EUR][1000 genomes]
rs9388649	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9388650	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9402055	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9482892	1.00[ASN][1000 genomes]
rs9482893	1.00[ASN][1000 genomes]
rs9482897	1.00[ASN][1000 genomes]
rs9482902	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9482904	1.00[ASN][1000 genomes]
rs9491988	1.00[ASN][1000 genomes]
rs9492000	0.85[CEU][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9492001	0.85[MEX][hapmap]
rs9492002	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.82[MEX][hapmap];0.92[TSI][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9492003	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9492004	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9492005	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9492008	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9492011	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9492013	1.00[ASN][1000 genomes]
rs9492014	1.00[ASN][1000 genomes]
rs9492017	1.00[CEU][hapmap];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9492020	1.00[ASN][1000 genomes]
rs9492021	1.00[CHD][hapmap];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1020071	chr6:128579774-129048919	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv538441	chr6:128579774-129048919	Flanking Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv830801	chr6:128878436-129064667	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs9492018	SAMD3	cis	parietal	SCAN
rs9492018	RSPO3	cis	cerebellum	SCAN
rs9492018	CHORDC1	trans	parietal	SCAN
rs9492018	C6orf174	cis	parietal	SCAN

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:128905400-128916000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:128906600-128908800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr6:128906800-128908000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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