Variant report

Variant	rs206253
Chromosome Location	chr3:162661026-162661027
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 165 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:138)

rs_ID	r²[population]
rs1027079	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1027081	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1157780	0.80[ASN][1000 genomes]
rs11708177	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11708229	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11712205	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11712339	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11712345	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11712346	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11716892	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12496047	0.81[ASN][1000 genomes]
rs12632097	0.80[ASN][1000 genomes]
rs13067606	0.81[AMR][1000 genomes]
rs13073109	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13077038	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13077542	0.81[ASN][1000 genomes]
rs13077678	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13084207	0.80[ASN][1000 genomes]
rs13090583	0.81[AMR][1000 genomes]
rs13099719	0.82[ASN][1000 genomes]
rs13100199	0.81[ASN][1000 genomes]
rs13318277	0.83[ASN][1000 genomes]
rs1386857	0.83[ASN][1000 genomes]
rs1386859	0.83[ASN][1000 genomes]
rs1386860	0.83[ASN][1000 genomes]
rs1386867	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1488169	0.83[ASN][1000 genomes]
rs1488170	0.83[ASN][1000 genomes]
rs1488171	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1488173	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1488178	0.83[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs1488179	0.88[ASN][1000 genomes]
rs1488180	0.80[ASN][1000 genomes]
rs1548001	0.83[ASN][1000 genomes]
rs1548002	0.83[ASN][1000 genomes]
rs1580514	0.80[ASN][1000 genomes]
rs1580515	0.80[ASN][1000 genomes]
rs1586501	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1844074	0.83[ASN][1000 genomes]
rs1844075	0.83[ASN][1000 genomes]
rs1946342	0.83[ASN][1000 genomes]
rs2046697	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2046698	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs206251	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs206254	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2114021	0.83[ASN][1000 genomes]
rs2129837	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2129838	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2129840	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2217021	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2362561	0.83[ASN][1000 genomes]
rs2541732	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34643571	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34894556	0.80[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs34942202	0.84[AMR][1000 genomes]
rs35095720	0.81[AMR][1000 genomes]
rs35264790	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35895206	0.82[AMR][1000 genomes]
rs3844503	0.89[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs4256162	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4260465	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4315704	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4325940	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4447790	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4450842	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4450843	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4462994	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4465967	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4467484	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4515074	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4538400	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4550841	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4579037	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4586839	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4616668	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4635732	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs60130055	0.80[ASN][1000 genomes]
rs61207972	0.81[ASN][1000 genomes]
rs62396436	0.83[ASN][1000 genomes]
rs6419710	0.84[AMR][1000 genomes]
rs6548346	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6548347	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6764040	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6773626	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6774016	0.80[ASN][1000 genomes]
rs6776179	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6780933	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6781129	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6790172	0.83[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs6798456	0.80[ASN][1000 genomes]
rs7355808	0.89[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs7427593	0.84[AMR][1000 genomes]
rs7614227	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7615072	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7615093	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7619891	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7626415	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7626416	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7626427	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7627448	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7629313	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7630728	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7631917	0.91[ASN][1000 genomes]
rs7633057	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7634239	0.81[AMR][1000 genomes]
rs7640988	0.89[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs7642473	0.81[AMR][1000 genomes]
rs7648102	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7650297	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9647385	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9681460	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9682007	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9682287	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9682612	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9682859	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9682872	0.88[AMR][1000 genomes]
rs9682874	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9682941	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9798973	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs981916	0.83[ASN][1000 genomes]
rs981917	0.83[ASN][1000 genomes]
rs981918	0.83[ASN][1000 genomes]
rs9820439	0.83[ASN][1000 genomes]
rs9822393	0.83[ASN][1000 genomes]
rs9822721	0.83[ASN][1000 genomes]
rs9852069	0.83[ASN][1000 genomes]
rs9858617	0.82[ASN][1000 genomes]
rs9858618	0.82[ASN][1000 genomes]
rs9858779	0.82[ASN][1000 genomes]
rs9860284	0.83[ASN][1000 genomes]
rs9863458	0.81[ASN][1000 genomes]
rs9864520	0.80[ASN][1000 genomes]
rs9866542	0.83[ASN][1000 genomes]
rs9867485	0.89[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs9869731	0.83[ASN][1000 genomes]
rs9870585	0.83[ASN][1000 genomes]
rs9877942	0.83[ASN][1000 genomes]
rs9879670	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428424	chr3:162145988-163033943	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv592201	chr3:162188625-163142162	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv470994	chr3:162217993-162945834	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv869804	chr3:162414099-162776884	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv2757902	chr3:162471049-162742794	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	esv2759197	chr3:162471049-162742794	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv869992	chr3:162483397-162776884	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv870318	chr3:162494699-162819441	Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv592214	chr3:162504321-162721962	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
10	nsv870056	chr3:162504822-162689567	Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
11	nsv592249	chr3:162512683-162721962	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
12	nsv592250	chr3:162512683-162768964	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	esv1813805	chr3:162513755-162721962	Enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Strong transcription Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
14	nsv829777	chr3:162515887-162677704	Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Strong transcription Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
15	nsv1000473	chr3:162545704-162673567	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
16	nsv536784	chr3:162545705-162677693	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
17	nsv1000858	chr3:162545705-162894644	Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
18	nsv829778	chr3:162565661-162732355	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
19	nsv877775	chr3:162595758-162735677	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
20	nsv877776	chr3:162618885-162671443	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
21	nsv877777	chr3:162618885-162727247	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
22	nsv877778	chr3:162618885-162754958	Enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
23	nsv877779	chr3:162618885-162932624	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
24	nsv877780	chr3:162618885-162935109	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
25	nsv1006015	chr3:162626560-163159978	Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
26	nsv1008026	chr3:162628602-162726677	ZNF genes & repeats Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
27	esv33448	chr3:162652132-162697412	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:162634400-162662200	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr3:162648400-162662400	Weak transcription	Aorta	Aorta
3	chr3:162654400-162665200	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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