Variant report

Variant	rs34669814
Chromosome Location	chr2:187039288-187039289
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 128 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:115)

rs_ID	r²[population]
rs10153530	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10173075	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10173730	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10175720	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10185816	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10185821	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10186061	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10193227	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10194241	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10195099	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10196449	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10497667	0.89[ASN][1000 genomes]
rs10931228	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12233005	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12233006	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12327903	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12327910	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12614595	0.89[ASN][1000 genomes]
rs12615895	0.89[ASN][1000 genomes]
rs12616722	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13388196	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13389991	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13394129	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13399174	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13401611	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13407103	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13419562	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13421172	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13424906	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13425057	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13428953	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13429238	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs16827536	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs16827550	0.87[ASN][1000 genomes]
rs16827554	0.86[ASN][1000 genomes]
rs16827557	0.86[ASN][1000 genomes]
rs16827559	0.86[ASN][1000 genomes]
rs16827564	0.86[ASN][1000 genomes]
rs16827586	0.86[ASN][1000 genomes]
rs16827590	0.85[ASN][1000 genomes]
rs16827599	0.86[ASN][1000 genomes]
rs16827602	0.86[ASN][1000 genomes]
rs16827614	0.82[ASN][1000 genomes]
rs1879430	0.80[ASN][1000 genomes]
rs1996506	0.82[ASN][1000 genomes]
rs1996507	0.81[ASN][1000 genomes]
rs1996508	0.82[ASN][1000 genomes]
rs2370660	0.81[ASN][1000 genomes]
rs2370668	0.82[ASN][1000 genomes]
rs2370669	0.82[ASN][1000 genomes]
rs2370670	0.84[ASN][1000 genomes]
rs2370671	0.86[ASN][1000 genomes]
rs2370672	0.86[ASN][1000 genomes]
rs2370674	0.86[ASN][1000 genomes]
rs2370676	0.87[ASN][1000 genomes]
rs2370677	0.88[ASN][1000 genomes]
rs2370678	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2370679	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2370680	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2370681	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2887816	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2887817	0.80[ASN][1000 genomes]
rs2887818	0.80[ASN][1000 genomes]
rs3107170	0.80[ASN][1000 genomes]
rs3107172	0.83[ASN][1000 genomes]
rs3107173	0.83[ASN][1000 genomes]
rs3107174	0.83[ASN][1000 genomes]
rs3107176	0.81[ASN][1000 genomes]
rs3107415	0.82[ASN][1000 genomes]
rs3107416	0.82[ASN][1000 genomes]
rs3107417	0.82[ASN][1000 genomes]
rs3107418	0.82[ASN][1000 genomes]
rs3107419	0.82[ASN][1000 genomes]
rs3107422	0.80[ASN][1000 genomes]
rs3107423	0.80[ASN][1000 genomes]
rs3107424	0.80[ASN][1000 genomes]
rs3107429	0.80[ASN][1000 genomes]
rs3112300	0.83[ASN][1000 genomes]
rs3112304	0.80[ASN][1000 genomes]
rs3112305	0.80[ASN][1000 genomes]
rs3112307	0.80[ASN][1000 genomes]
rs3112318	0.83[ASN][1000 genomes]
rs3112319	0.83[ASN][1000 genomes]
rs34113619	0.88[ASN][1000 genomes]
rs34133588	0.88[ASN][1000 genomes]
rs34176985	0.89[ASN][1000 genomes]
rs34627487	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34651427	0.86[ASN][1000 genomes]
rs35156447	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35252434	0.88[ASN][1000 genomes]
rs35298515	0.89[ASN][1000 genomes]
rs35504474	0.86[ASN][1000 genomes]
rs35522677	0.89[ASN][1000 genomes]
rs35567611	0.86[ASN][1000 genomes]
rs35590244	0.89[ASN][1000 genomes]
rs35652084	0.84[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs35942256	0.88[ASN][1000 genomes]
rs4284795	0.89[ASN][1000 genomes]
rs4338930	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4417686	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4461230	0.86[ASN][1000 genomes]
rs4591314	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4614896	0.88[ASN][1000 genomes]
rs4643502	0.86[ASN][1000 genomes]
rs57423042	0.82[AMR][1000 genomes]
rs61573398	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs72903625	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs72903626	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs72905629	0.87[ASN][1000 genomes]
rs72907517	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7569990	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7584724	0.86[ASN][1000 genomes]
rs8179713	0.89[ASN][1000 genomes]
rs9288123	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9288124	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv875545	chr2:186566024-187280164	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv817325	chr2:186625679-187200841	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv868949	chr2:186657142-187327560	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv1002243	chr2:186692815-187150225	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv536077	chr2:186692815-187150225	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv932296	chr2:186737443-187265790	Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
7	nsv875548	chr2:186798249-187164657	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv1003369	chr2:186980675-187133740	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv961702	chr2:187027942-187043962	ZNF genes & repeats Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv1014726	chr2:187036909-187213113	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
11	nsv536078	chr2:187036909-187213113	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
12	esv3409453	chr2:187038157-187040355	Weak transcription	n/a	n/a	inside rSNPs	diseases
13	esv3420478	chr2:187038657-187039955	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:187025000-187049800	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr2:187029400-187044400	Weak transcription	Aorta	Aorta

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