Variant report

Variant	rs9832758
Chromosome Location	chr3:80781447-80781448
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs12485625	0.82[AMR][1000 genomes]
rs13060063	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13066372	0.80[ASN][1000 genomes]
rs13078405	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13094364	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1320909	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1320910	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13318177	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13324031	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1399556	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1406784	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1437046	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1515004	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1516585	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1520589	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1520590	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17280627	0.82[AFR][1000 genomes]
rs1996224	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2037094	0.84[EUR][1000 genomes]
rs2049778	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2056084	0.83[EUR][1000 genomes]
rs2139685	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2176029	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2372654	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2372655	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2372656	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2372657	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2372660	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs28490262	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28885819	0.89[AFR][1000 genomes]
rs4270470	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs500298	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs528897	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs571776	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs584597	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs588001	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs613707	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs619305	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62258009	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62258010	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs627529	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6548716	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6548719	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs704464	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7431461	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7617921	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7621792	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7630983	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7630997	0.84[EUR][1000 genomes]
rs7631866	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7631989	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7633466	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7633748	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7639808	0.82[AMR][1000 genomes]
rs7643304	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs878245	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs966619	0.85[EUR][1000 genomes]
rs9818650	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1004115	chr3:80349665-81043308	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv536601	chr3:80349665-81043308	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv1067580	chr3:80416729-81043307	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv492220	chr3:80416729-81043307	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv1000592	chr3:80422155-81044175	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	nsv527598	chr3:80585455-81250663	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	nsv877037	chr3:80611818-80811252	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:80780600-80785600	Enhancers	HUVEC	blood vessel
2	chr3:80781000-80784800	Enhancers	Fetal Intestine Large	intestine
3	chr3:80781400-80781600	Enhancers	Fetal Intestine Small	intestine
4	chr3:80781400-80782600	Enhancers	Hela-S3	cervix

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