Variant report

Variant	rs35516514
Chromosome Location	chr8:51142383-51142384
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 93 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:91)

rs_ID	r²[population]
rs10094935	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10108468	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10504098	0.82[AMR][1000 genomes]
rs10504099	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10957813	0.80[AMR][1000 genomes]
rs10957814	0.82[AMR][1000 genomes]
rs10957853	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1160764	0.80[ASN][1000 genomes]
rs1160795	0.80[ASN][1000 genomes]
rs11775978	0.80[AMR][1000 genomes]
rs11780070	0.82[AMR][1000 genomes]
rs11781981	0.83[AMR][1000 genomes]
rs11784464	0.80[ASN][1000 genomes]
rs11786703	0.83[AMR][1000 genomes]
rs12056425	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12056426	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12544631	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12545365	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12545915	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12677522	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12677964	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12678703	0.83[ASN][1000 genomes]
rs12679317	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12679356	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13251587	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13277538	0.82[AMR][1000 genomes]
rs1450127	0.86[EUR][1000 genomes]
rs1597428	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1597429	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1597430	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1597431	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs16914376	0.82[AMR][1000 genomes]
rs16914459	0.83[AMR][1000 genomes]
rs1901050	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2084590	0.85[EUR][1000 genomes]
rs2084591	0.85[EUR][1000 genomes]
rs28510664	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34217744	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34651805	0.80[ASN][1000 genomes]
rs34722367	0.82[AMR][1000 genomes]
rs34788367	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34908431	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs34997857	0.84[AMR][1000 genomes]
rs35857674	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs36006902	0.82[AMR][1000 genomes]
rs4448283	0.85[EUR][1000 genomes]
rs4448284	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4873126	0.83[AMR][1000 genomes]
rs4873127	0.83[AMR][1000 genomes]
rs4873128	0.82[AMR][1000 genomes]
rs4873129	0.80[AMR][1000 genomes]
rs4873131	0.84[EUR][1000 genomes]
rs4873132	0.85[EUR][1000 genomes]
rs4873133	0.85[EUR][1000 genomes]
rs4873134	0.85[EUR][1000 genomes]
rs4873135	0.85[EUR][1000 genomes]
rs4873141	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4873143	0.80[ASN][1000 genomes]
rs4873412	0.80[AMR][1000 genomes]
rs4873413	0.82[AMR][1000 genomes]
rs4873414	0.80[AMR][1000 genomes]
rs4873415	0.83[AMR][1000 genomes]
rs4873416	0.82[AMR][1000 genomes]
rs4873418	0.82[AMR][1000 genomes]
rs4873426	0.84[EUR][1000 genomes]
rs4873427	0.85[EUR][1000 genomes]
rs4873428	0.85[EUR][1000 genomes]
rs4873438	0.80[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4873439	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56007637	0.80[AMR][1000 genomes]
rs62516672	0.83[AMR][1000 genomes]
rs62516685	0.82[AMR][1000 genomes]
rs62516687	0.82[AMR][1000 genomes]
rs6983498	0.85[EUR][1000 genomes]
rs7000325	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7002235	0.80[AMR][1000 genomes]
rs7003725	0.80[ASN][1000 genomes]
rs7010037	0.82[AMR][1000 genomes]
rs7018082	0.84[EUR][1000 genomes]
rs7464491	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7817040	0.84[EUR][1000 genomes]
rs7817638	0.84[EUR][1000 genomes]
rs7821189	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7822550	0.80[ASN][1000 genomes]
rs7824938	0.82[AMR][1000 genomes]
rs7825053	0.82[AMR][1000 genomes]
rs7835849	0.84[EUR][1000 genomes]
rs870754	0.84[AMR][1000 genomes]
rs884561	0.82[AMR][1000 genomes]
rs898520	0.80[AMR][1000 genomes]
rs9298295	0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916392	chr8:50827638-51395140	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv948436	chr8:51115028-51917504	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:51142000-51143200	Enhancers	Liver	Liver

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