Variant report

Variant	rs11921692
Chromosome Location	chr3:28436281-28436282
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 119 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:116)

rs_ID	r²[population]
rs1037723	0.95[ASN][1000 genomes]
rs11705962	0.91[ASN][1000 genomes]
rs11706332	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[ASN][1000 genomes]
rs11707705	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11710963	0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11712484	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs11712489	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs11720107	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11918050	1.00[CEU][hapmap];0.92[CHB][hapmap];0.86[JPT][hapmap];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11921943	1.00[CHB][hapmap]
rs11924173	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11926399	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12107256	0.84[CHB][hapmap]
rs13066118	0.89[ASN][1000 genomes]
rs13074633	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13075840	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13080155	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13081520	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13081787	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13082167	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap]
rs13083544	0.84[CHB][hapmap]
rs13085075	1.00[CHB][hapmap]
rs13087143	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13087774	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13088574	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.96[YRI][hapmap];0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13090296	0.84[CHB][hapmap]
rs13090439	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13093242	0.84[CHB][hapmap]
rs13095628	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13095675	1.00[CHB][hapmap]
rs13099152	0.85[ASN][1000 genomes]
rs1457909	0.92[ASN][1000 genomes]
rs1457910	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1585211	1.00[CHB][hapmap]
rs1598846	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap]
rs1599826	0.92[CHB][hapmap]
rs1606386	0.88[CEU][hapmap];0.92[CHB][hapmap];0.86[ASN][1000 genomes]
rs1606388	0.91[CEU][hapmap];0.92[CHB][hapmap];0.81[ASN][1000 genomes]
rs1610238	0.84[CHB][hapmap]
rs17021306	0.84[CHB][hapmap]
rs17021402	0.96[CEU][hapmap];0.93[CHB][hapmap];0.86[JPT][hapmap];0.97[YRI][hapmap];0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17357206	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17638742	0.91[CEU][hapmap];0.92[CHB][hapmap];0.85[ASN][1000 genomes]
rs17638782	0.85[ASN][1000 genomes]
rs17638991	0.95[CEU][hapmap];1.00[CHB][hapmap];0.86[ASN][1000 genomes]
rs17639978	0.95[CEU][hapmap];0.92[EUR][1000 genomes]
rs17695765	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.86[ASN][1000 genomes]
rs17695884	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17696025	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17696459	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17696561	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17696783	0.91[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.95[ASN][1000 genomes]
rs1870259	1.00[CHB][hapmap]
rs2168799	1.00[CHB][hapmap]
rs34311197	0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34574968	0.86[ASN][1000 genomes]
rs34796684	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35088087	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35137555	0.92[ASN][1000 genomes]
rs35177150	0.95[ASN][1000 genomes]
rs35702956	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35736614	0.85[ASN][1000 genomes]
rs35825908	0.95[ASN][1000 genomes]
rs35845822	0.85[ASN][1000 genomes]
rs36051688	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36105900	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3762797	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4234337	0.90[ASN][1000 genomes]
rs4234338	0.83[CHB][hapmap]
rs4256085	0.90[ASN][1000 genomes]
rs4295137	0.90[ASN][1000 genomes]
rs4322963	0.89[ASN][1000 genomes]
rs4428136	0.88[ASN][1000 genomes]
rs4450765	0.90[ASN][1000 genomes]
rs4452283	0.96[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4522735	0.85[ASN][1000 genomes]
rs4680753	0.90[ASN][1000 genomes]
rs4680909	1.00[CHB][hapmap]
rs4680913	1.00[CHB][hapmap];0.80[ASN][1000 genomes]
rs58918848	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59975750	0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs60043893	0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62250271	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62250272	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62250273	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62250296	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62251105	0.86[ASN][1000 genomes]
rs62251108	0.84[ASN][1000 genomes]
rs62251131	0.96[ASN][1000 genomes]
rs62251134	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62251138	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62251144	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62252069	0.85[ASN][1000 genomes]
rs6551255	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66733194	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs66767946	0.91[ASN][1000 genomes]
rs6771057	1.00[CHB][hapmap]
rs6771460	0.96[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.97[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6803692	1.00[CHB][hapmap]
rs68085718	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71087683	0.85[ASN][1000 genomes]
rs7434193	0.95[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7627471	0.88[ASN][1000 genomes]
rs7627575	0.90[ASN][1000 genomes]
rs7635383	0.86[ASN][1000 genomes]
rs7638450	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7639750	1.00[CHB][hapmap]
rs7641491	1.00[CHB][hapmap]
rs7643191	0.91[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.92[ASN][1000 genomes]
rs7649498	1.00[CHB][hapmap]
rs7650831	0.83[ASN][1000 genomes]
rs7651883	1.00[CHB][hapmap];0.80[ASN][1000 genomes]
rs952888	0.86[CEU][hapmap];0.85[ASN][1000 genomes]
rs9683360	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs969443	0.92[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.95[ASN][1000 genomes]
rs9843464	1.00[CHB][hapmap]

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	esv3328565	chr3:27991169-28915035	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv876649	chr3:28126595-28718454	Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv876650	chr3:28427029-28613602	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr3:28433400-28441000	Weak transcription	Right Ventricle	heart

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