Variant report

Variant	rs6769733
Chromosome Location	chr3:50933638-50933639
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 184 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:181)

rs_ID	r²[population]
rs10510754	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10865962	0.93[CEU][hapmap]
rs11130255	0.93[CEU][hapmap]
rs11130263	0.93[CEU][hapmap]
rs11130267	0.93[CEU][hapmap]
rs11710858	0.94[CEU][hapmap]
rs11712367	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs11715556	0.94[CEU][hapmap]
rs11917538	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11919932	0.93[CEU][hapmap]
rs11921011	0.93[CEU][hapmap]
rs11928733	0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12639126	0.94[CEU][hapmap]
rs12639243	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13061003	1.00[CEU][hapmap]
rs13062018	0.93[CEU][hapmap]
rs13064199	0.93[CEU][hapmap]
rs13065995	0.93[CEU][hapmap]
rs13069365	0.81[CEU][hapmap]
rs13075377	0.93[CEU][hapmap]
rs13079136	0.94[CEU][hapmap]
rs13079565	0.94[CEU][hapmap]
rs13080170	1.00[CEU][hapmap]
rs13085827	0.93[CEU][hapmap]
rs13086922	0.93[CEU][hapmap]
rs13088434	0.94[CEU][hapmap]
rs13093289	0.93[CEU][hapmap]
rs13093798	0.93[CEU][hapmap]
rs13095920	0.94[CEU][hapmap]
rs13324500	0.94[CEU][hapmap]
rs1379875	0.94[CEU][hapmap]
rs1458385	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1458386	0.93[CEU][hapmap]
rs1458387	0.94[CEU][hapmap]
rs1463496	0.94[CEU][hapmap]
rs1463497	0.94[CEU][hapmap]
rs1471177	0.94[CEU][hapmap]
rs1531271	0.94[CEU][hapmap]
rs1598926	0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17660513	0.92[CEU][hapmap]
rs1824280	0.94[CEU][hapmap]
rs1824281	0.94[CEU][hapmap]
rs1947607	0.93[CEU][hapmap]
rs1966920	0.93[CEU][hapmap]
rs2045510	0.94[CEU][hapmap]
rs2045511	0.94[CEU][hapmap]
rs2061388	0.94[CEU][hapmap]
rs2085580	0.93[CEU][hapmap]
rs2085582	0.93[CEU][hapmap]
rs2125366	0.94[CEU][hapmap]
rs2125369	0.94[CEU][hapmap]
rs2168863	0.94[CEU][hapmap]
rs2168866	0.93[CEU][hapmap]
rs2199050	0.94[CEU][hapmap]
rs2219431	0.93[CEU][hapmap]
rs2219432	0.94[CEU][hapmap]
rs2219433	0.93[CEU][hapmap]
rs2262810	0.94[CEU][hapmap]
rs2355350	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2355697	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2355700	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2355702	0.94[CEU][hapmap]
rs2608988	0.93[CEU][hapmap]
rs2609001	0.94[CEU][hapmap]
rs2609006	0.93[CEU][hapmap]
rs2609020	0.94[CEU][hapmap]
rs2609022	0.93[CEU][hapmap]
rs2609024	0.93[CEU][hapmap]
rs2609031	0.93[CEU][hapmap]
rs2609036	0.94[CEU][hapmap]
rs2609037	0.94[CEU][hapmap]
rs2675772	0.94[CEU][hapmap]
rs2675773	0.94[CEU][hapmap]
rs2675792	0.93[CEU][hapmap]
rs2675806	0.93[CEU][hapmap]
rs2675810	0.87[CEU][hapmap]
rs2675812	0.94[CEU][hapmap]
rs2675816	0.90[CEU][hapmap]
rs2675830	0.93[CEU][hapmap]
rs2675832	0.93[CEU][hapmap]
rs2675834	0.94[CEU][hapmap]
rs2675835	0.93[CEU][hapmap]
rs2675836	0.93[CEU][hapmap]
rs2675837	0.94[CEU][hapmap]
rs2883652	0.94[CEU][hapmap]
rs34628582	0.93[CEU][hapmap]
rs4132022	0.87[CEU][hapmap]
rs4244704	0.93[CEU][hapmap]
rs4263323	0.93[CEU][hapmap]
rs4346541	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4346542	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4373098	0.93[CEU][hapmap]
rs4377512	0.93[CEU][hapmap]
rs4429624	0.93[CEU][hapmap]
rs4438692	0.93[CEU][hapmap]
rs4443210	1.00[CEU][hapmap]
rs4446244	0.93[CEU][hapmap]
rs4447760	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4482663	0.93[CEU][hapmap]
rs4485709	1.00[CEU][hapmap]
rs4488874	0.93[CEU][hapmap]
rs4505743	0.94[CEU][hapmap]
rs4511931	0.93[CEU][hapmap]
rs4511933	0.93[CEU][hapmap]
rs4530518	0.92[CEU][hapmap]
rs4530566	0.93[CEU][hapmap]
rs4555554	0.94[CEU][hapmap]
rs4566574	0.94[CEU][hapmap]
rs4572801	1.00[CEU][hapmap]
rs4582086	0.93[CEU][hapmap]
rs4586853	0.93[CEU][hapmap]
rs4615113	0.93[CEU][hapmap]
rs4688702	0.93[CEU][hapmap]
rs4927960	0.93[CEU][hapmap]
rs61108141	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6445600	0.93[CEU][hapmap]
rs6445717	0.94[CEU][hapmap]
rs6445750	0.93[CEU][hapmap]
rs6445779	0.94[CEU][hapmap]
rs6445802	0.90[CEU][hapmap]
rs6446212	0.93[CEU][hapmap]
rs6446213	0.93[CEU][hapmap]
rs6446214	0.87[CEU][hapmap]
rs6446220	1.00[CEU][hapmap];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6446222	1.00[CEU][hapmap];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6446243	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6446245	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6768601	0.93[CEU][hapmap]
rs6771085	0.93[CEU][hapmap]
rs6775012	0.93[CEU][hapmap]
rs6776224	0.93[CEU][hapmap]
rs6778680	0.93[CEU][hapmap]
rs6787773	0.93[CEU][hapmap]
rs6795272	0.93[CEU][hapmap]
rs6795573	1.00[CEU][hapmap];0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6810241	0.93[CEU][hapmap]
rs7428086	0.93[CEU][hapmap]
rs7429035	0.93[CEU][hapmap]
rs7433217	1.00[CEU][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7611428	0.93[CEU][hapmap]
rs7611873	0.94[CEU][hapmap]
rs7614171	0.94[CEU][hapmap]
rs7614482	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7614881	0.93[CEU][hapmap]
rs7615703	0.93[CEU][hapmap]
rs7616183	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7621650	0.90[EUR][1000 genomes]
rs7627266	1.00[CEU][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7629253	0.93[CEU][hapmap]
rs7629420	0.93[CEU][hapmap]
rs7638082	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7638732	0.93[CEU][hapmap]
rs7639301	0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7639828	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7642158	0.93[CEU][hapmap]
rs7650574	0.94[CEU][hapmap]
rs7652715	0.93[CEU][hapmap]
rs7653451	0.93[CEU][hapmap]
rs936405	0.93[CEU][hapmap]
rs936406	0.93[CEU][hapmap]
rs9682672	0.94[CEU][hapmap]
rs9713241	0.93[CEU][hapmap]
rs9758600	0.91[CEU][hapmap]
rs9823942	0.93[CEU][hapmap]
rs9824444	0.89[EUR][1000 genomes]
rs9824522	0.89[EUR][1000 genomes]
rs9825535	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs9826757	0.91[CEU][hapmap]
rs9832952	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9837334	1.00[CEU][hapmap]
rs9838283	0.94[CEU][hapmap]
rs9838433	0.85[AFR][1000 genomes];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9839684	0.90[CEU][hapmap]
rs9850021	0.93[CEU][hapmap]
rs9857727	0.94[CEU][hapmap]
rs9859692	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9867489	0.87[EUR][1000 genomes]
rs9868870	0.93[CEU][hapmap]
rs9869945	1.00[CEU][hapmap];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9875961	1.00[CEU][hapmap];0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9877272	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[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	nsv491647	chr3:50856276-51245158	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1004881	chr3:50900793-51032918	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv536568	chr3:50900793-51032918	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr3:50931400-50938200	Weak transcription	H9 Cell Line	embryonic stem cell

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