Variant report

Variant	rs1990672
Chromosome Location	chr3:34691773-34691774
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 98 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:94)

rs_ID	r²[population]
rs10510660	1.00[ASN][1000 genomes]
rs10865859	0.91[ASN][1000 genomes]
rs1117173	0.91[ASN][1000 genomes]
rs1117663	0.90[ASN][1000 genomes]
rs11525737	0.92[ASN][1000 genomes]
rs11525738	0.90[ASN][1000 genomes]
rs11705846	0.90[ASN][1000 genomes]
rs11708235	0.88[ASN][1000 genomes]
rs11712215	0.88[ASN][1000 genomes]
rs11715912	0.88[ASN][1000 genomes]
rs11716705	0.84[ASN][1000 genomes]
rs11716737	0.88[ASN][1000 genomes]
rs11718900	0.88[ASN][1000 genomes]
rs11719003	0.88[ASN][1000 genomes]
rs11721181	0.88[ASN][1000 genomes]
rs11916603	0.87[ASN][1000 genomes]
rs11919593	0.88[ASN][1000 genomes]
rs12233438	0.92[ASN][1000 genomes]
rs12486760	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12487200	0.91[ASN][1000 genomes]
rs12491003	0.84[ASN][1000 genomes]
rs12492940	0.91[ASN][1000 genomes]
rs12636214	0.92[ASN][1000 genomes]
rs12636313	0.89[ASN][1000 genomes]
rs13058934	0.91[ASN][1000 genomes]
rs13059811	0.90[ASN][1000 genomes]
rs13060690	0.90[ASN][1000 genomes]
rs13066312	0.91[ASN][1000 genomes]
rs13066328	0.91[ASN][1000 genomes]
rs13072344	0.86[ASN][1000 genomes]
rs13072842	0.90[ASN][1000 genomes]
rs13080033	0.92[ASN][1000 genomes]
rs13080219	0.92[ASN][1000 genomes]
rs13082790	0.84[ASN][1000 genomes]
rs13085801	0.91[ASN][1000 genomes]
rs13088951	0.88[ASN][1000 genomes]
rs13089465	0.88[ASN][1000 genomes]
rs1468835	0.88[ASN][1000 genomes]
rs1520632	0.90[ASN][1000 genomes]
rs1520645	0.90[ASN][1000 genomes]
rs1581333	0.88[ASN][1000 genomes]
rs1589338	0.88[ASN][1000 genomes]
rs1607771	0.90[ASN][1000 genomes]
rs1607773	0.88[ASN][1000 genomes]
rs1851058	0.88[ASN][1000 genomes]
rs1966433	0.88[ASN][1000 genomes]
rs2011180	0.88[ASN][1000 genomes]
rs2080424	0.90[ASN][1000 genomes]
rs2098399	0.88[ASN][1000 genomes]
rs2193080	0.90[ASN][1000 genomes]
rs2216183	0.88[ASN][1000 genomes]
rs2358501	0.91[ASN][1000 genomes]
rs2358502	0.88[ASN][1000 genomes]
rs28505771	0.88[ASN][1000 genomes]
rs34913545	0.89[ASN][1000 genomes]
rs35241516	0.90[ASN][1000 genomes]
rs35952247	0.89[ASN][1000 genomes]
rs4465892	0.88[ASN][1000 genomes]
rs4467396	0.90[ASN][1000 genomes]
rs4572717	0.88[ASN][1000 genomes]
rs4678700	0.88[ASN][1000 genomes]
rs55722413	0.87[ASN][1000 genomes]
rs59785806	0.88[ASN][1000 genomes]
rs60107689	0.90[ASN][1000 genomes]
rs6550286	0.90[ASN][1000 genomes]
rs66511672	0.91[ASN][1000 genomes]
rs6762092	0.86[ASN][1000 genomes]
rs6762310	0.90[ASN][1000 genomes]
rs6764675	0.91[ASN][1000 genomes]
rs6766288	0.90[ASN][1000 genomes]
rs6770132	0.88[ASN][1000 genomes]
rs6770932	0.88[ASN][1000 genomes]
rs6779356	0.91[ASN][1000 genomes]
rs6794876	0.88[ASN][1000 genomes]
rs6799362	0.87[ASN][1000 genomes]
rs6799370	0.88[ASN][1000 genomes]
rs6799746	0.90[ASN][1000 genomes]
rs6806506	0.88[ASN][1000 genomes]
rs6806757	0.88[ASN][1000 genomes]
rs7614543	0.88[ASN][1000 genomes]
rs7624543	0.91[ASN][1000 genomes]
rs7624853	0.91[ASN][1000 genomes]
rs7632406	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7637897	0.90[ASN][1000 genomes]
rs7639229	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7639870	0.91[ASN][1000 genomes]
rs7643365	0.89[ASN][1000 genomes]
rs7649251	0.88[ASN][1000 genomes]
rs7650207	0.91[ASN][1000 genomes]
rs918086	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs974687	0.88[ASN][1000 genomes]
rs9809734	0.90[ASN][1000 genomes]
rs9878478	0.88[ASN][1000 genomes]
rs9878670	0.88[ASN][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	esv1820420	chr3:34662157-34708263	Enhancers Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
2	esv1822284	chr3:34683998-34692545	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
3	nsv519548	chr3:34683998-34718800	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
4	esv1816528	chr3:34683998-34757534	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:34691400-34692000	Enhancers	Fetal Heart	heart

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