Variant report

Variant	rs34894556
Chromosome Location	chr3:162682303-162682304
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 122 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:92)

rs_ID	r²[population]
rs1030362	0.81[ASN][1000 genomes]
rs1038634	0.81[ASN][1000 genomes]
rs1038635	0.82[ASN][1000 genomes]
rs1157780	0.83[ASN][1000 genomes]
rs11716892	0.92[ASN][1000 genomes]
rs12489054	0.83[ASN][1000 genomes]
rs12496047	0.85[ASN][1000 genomes]
rs12632097	0.83[ASN][1000 genomes]
rs13073109	0.94[ASN][1000 genomes]
rs13077542	0.85[ASN][1000 genomes]
rs13084207	0.83[ASN][1000 genomes]
rs13099719	0.86[ASN][1000 genomes]
rs13100199	0.84[ASN][1000 genomes]
rs13318277	0.86[ASN][1000 genomes]
rs1386857	0.86[ASN][1000 genomes]
rs1386859	0.86[ASN][1000 genomes]
rs1386860	0.86[ASN][1000 genomes]
rs1386867	0.87[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs1488169	0.86[ASN][1000 genomes]
rs1488170	0.86[ASN][1000 genomes]
rs1488171	0.94[ASN][1000 genomes]
rs1488173	0.84[ASN][1000 genomes]
rs1488178	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1488179	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1488180	0.83[ASN][1000 genomes]
rs1488181	0.82[ASN][1000 genomes]
rs1548001	0.86[ASN][1000 genomes]
rs1548002	0.86[ASN][1000 genomes]
rs1580514	0.83[ASN][1000 genomes]
rs1580515	0.83[ASN][1000 genomes]
rs1586501	0.81[ASN][1000 genomes]
rs1844074	0.86[ASN][1000 genomes]
rs1844075	0.86[ASN][1000 genomes]
rs1946342	0.86[ASN][1000 genomes]
rs206251	0.87[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs206253	0.80[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs206254	0.80[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs206259	0.84[AMR][1000 genomes]
rs206263	0.84[AMR][1000 genomes]
rs2114021	0.86[ASN][1000 genomes]
rs2129837	0.81[ASN][1000 genomes]
rs2129838	0.81[ASN][1000 genomes]
rs2129841	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2217021	0.94[ASN][1000 genomes]
rs2362561	0.86[ASN][1000 genomes]
rs2362563	0.82[ASN][1000 genomes]
rs2541732	0.80[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs34643571	0.92[ASN][1000 genomes]
rs35136410	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs35264790	0.92[ASN][1000 genomes]
rs3844503	0.85[ASN][1000 genomes]
rs4515074	0.90[ASN][1000 genomes]
rs60130055	0.83[ASN][1000 genomes]
rs61207972	0.85[ASN][1000 genomes]
rs62396436	0.86[ASN][1000 genomes]
rs6548348	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6774016	0.83[ASN][1000 genomes]
rs6784221	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6790172	0.87[ASN][1000 genomes]
rs6798456	0.83[ASN][1000 genomes]
rs7355808	0.87[ASN][1000 genomes]
rs7615072	0.81[ASN][1000 genomes]
rs7617016	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7621784	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7627450	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7631917	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7640988	0.87[ASN][1000 genomes]
rs7648102	0.90[ASN][1000 genomes]
rs7650297	0.94[ASN][1000 genomes]
rs9681460	0.93[ASN][1000 genomes]
rs9682612	0.94[ASN][1000 genomes]
rs9682941	0.94[ASN][1000 genomes]
rs981916	0.86[ASN][1000 genomes]
rs981917	0.86[ASN][1000 genomes]
rs981918	0.86[ASN][1000 genomes]
rs9820439	0.86[ASN][1000 genomes]
rs9822393	0.86[ASN][1000 genomes]
rs9822721	0.86[ASN][1000 genomes]
rs9852069	0.86[ASN][1000 genomes]
rs9858129	0.83[ASN][1000 genomes]
rs9858617	0.85[ASN][1000 genomes]
rs9858618	0.85[ASN][1000 genomes]
rs9858779	0.85[ASN][1000 genomes]
rs9860284	0.86[ASN][1000 genomes]
rs9863458	0.85[ASN][1000 genomes]
rs9864520	0.83[ASN][1000 genomes]
rs9866542	0.86[ASN][1000 genomes]
rs9867485	0.86[ASN][1000 genomes]
rs9869731	0.86[ASN][1000 genomes]
rs9870585	0.86[ASN][1000 genomes]
rs9877942	0.86[ASN][1000 genomes]
rs9879670	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:30 , 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	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	esv33448	chr3:162652132-162697412	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
24	nsv877781	chr3:162664345-162754958	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
25	nsv877782	chr3:162664345-162918387	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
26	nsv877783	chr3:162678550-162719684	Active TSS Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
27	nsv877784	chr3:162678550-162733793	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
28	nsv877785	chr3:162678550-162737519	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
29	nsv877786	chr3:162678550-162754958	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
30	nsv877787	chr3:162678550-162809107	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr3:162681800-162682400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell

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