Variant report

Variant	rs2093434
Chromosome Location	chr10:96638857-96638858
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 126 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:111)

rs_ID	r²[population]
rs1042192	0.92[CEU][hapmap];0.88[CHB][hapmap];0.83[JPT][hapmap];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1042194	0.92[CEU][hapmap];0.94[CHB][hapmap];0.83[JPT][hapmap];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10509676	0.92[CEU][hapmap];0.94[CHB][hapmap];0.84[JPT][hapmap];0.93[YRI][hapmap];0.81[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs10509679	0.85[CEU][hapmap];0.88[CHB][hapmap];0.80[ASN][1000 genomes]
rs1074145	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12569735	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12569850	0.80[ASN][1000 genomes]
rs12571421	0.92[CEU][hapmap];0.94[CHB][hapmap];0.83[JPT][hapmap];0.92[YRI][hapmap];0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12571533	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12572071	0.80[ASN][1000 genomes]
rs12572085	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12572351	0.85[CEU][hapmap];0.88[CHB][hapmap];0.80[ASN][1000 genomes]
rs12572499	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12572588	0.80[ASN][1000 genomes]
rs12572917	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12573074	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12762136	0.81[EUR][1000 genomes]
rs12762370	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12763230	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12767583	0.85[CEU][hapmap];0.88[CHB][hapmap];0.83[JPT][hapmap];0.92[YRI][hapmap];0.83[AFR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12768009	0.92[CEU][hapmap];0.92[YRI][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12768857	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12769205	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12769684	0.80[ASN][1000 genomes]
rs12772672	0.92[CEU][hapmap];0.94[CHB][hapmap];0.83[JPT][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12773342	0.92[CEU][hapmap];0.94[CHB][hapmap];0.84[JPT][hapmap];0.93[YRI][hapmap]
rs12775283	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12775707	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12777311	0.83[EUR][1000 genomes]
rs12778026	0.92[CEU][hapmap];0.94[CHB][hapmap];0.84[JPT][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12778966	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12781477	0.81[EUR][1000 genomes]
rs12782374	0.80[ASN][1000 genomes]
rs12783288	0.80[ASN][1000 genomes]
rs12783509	0.83[EUR][1000 genomes]
rs12783988	0.83[EUR][1000 genomes]
rs12784219	0.83[EUR][1000 genomes]
rs12785038	0.82[AMR][1000 genomes]
rs12785201	0.80[ASN][1000 genomes]
rs1322179	0.92[CEU][hapmap];0.94[CHB][hapmap];0.83[JPT][hapmap];0.92[YRI][hapmap];0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1326832	0.92[CEU][hapmap];0.94[CHB][hapmap];0.84[JPT][hapmap];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1578438	0.80[ASN][1000 genomes]
rs1853205	0.92[CEU][hapmap];0.94[CHB][hapmap];0.84[JPT][hapmap];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1926711	0.81[EUR][1000 genomes]
rs1926712	0.92[CEU][hapmap];0.94[CHB][hapmap];0.83[JPT][hapmap];0.83[EUR][1000 genomes]
rs2181097	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2281890	0.92[CEU][hapmap];0.94[CHB][hapmap];0.83[JPT][hapmap];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2281891	0.92[CEU][hapmap];0.83[CHB][hapmap];0.83[JPT][hapmap];0.92[YRI][hapmap]
rs2296680	0.92[CEU][hapmap];0.94[CHB][hapmap];0.83[JPT][hapmap];0.81[EUR][1000 genomes]
rs2298037	0.85[CEU][hapmap];0.88[CHB][hapmap]
rs28399513	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2860838	0.92[CEU][hapmap];0.94[CHB][hapmap];0.83[JPT][hapmap]
rs2860903	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34058919	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs34121168	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34532201	0.80[ASN][1000 genomes]
rs34607361	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34777815	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs35059536	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs35126593	0.80[ASN][1000 genomes]
rs35172334	0.80[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs35390752	0.92[CEU][hapmap];0.94[CHB][hapmap];0.83[JPT][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35391887	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35406621	0.80[ASN][1000 genomes]
rs35626865	0.80[ASN][1000 genomes]
rs35709381	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs35751085	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35835168	0.81[EUR][1000 genomes]
rs3758580	0.92[CEU][hapmap];0.94[CHB][hapmap];0.84[JPT][hapmap];0.93[YRI][hapmap];0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3818504	0.81[EUR][1000 genomes]
rs4244285	0.92[CEU][hapmap];0.94[CHB][hapmap];0.84[JPT][hapmap];0.93[YRI][hapmap];0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4417205	0.92[CEU][hapmap];0.94[CHB][hapmap];0.84[JPT][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4445573	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4532967	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4589212	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4641393	0.92[CEU][hapmap];0.94[CHB][hapmap];0.83[JPT][hapmap];0.92[YRI][hapmap];0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4986894	0.92[CEU][hapmap];0.94[CHB][hapmap];0.88[JPT][hapmap];0.92[YRI][hapmap];0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs56229007	0.87[EUR][1000 genomes]
rs58335703	0.80[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs58447435	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6583954	0.92[CEU][hapmap];0.94[CHB][hapmap];0.83[JPT][hapmap];0.85[EUR][1000 genomes]
rs67120915	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7085563	0.81[CHB][hapmap];0.81[EUR][1000 genomes]
rs7085890	0.92[CEU][hapmap];0.94[CHB][hapmap];0.84[JPT][hapmap];0.80[EUR][1000 genomes]
rs7100783	0.92[CEU][hapmap];0.94[CHB][hapmap];0.88[JPT][hapmap];0.93[YRI][hapmap]
rs71482318	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs71482322	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs717238	0.92[CEU][hapmap];0.94[CHB][hapmap];0.83[JPT][hapmap]
rs72816654	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72818619	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7475739	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7897904	0.94[EUR][1000 genomes]
rs7900135	0.92[CEU][hapmap];0.94[CHB][hapmap];0.83[JPT][hapmap];0.81[EUR][1000 genomes]
rs7904581	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7910879	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7911008	0.87[EUR][1000 genomes]
rs7911654	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7919524	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs932809	0.92[CEU][hapmap];0.94[CHB][hapmap];0.83[JPT][hapmap];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9332105	0.85[CEU][hapmap];0.89[CHB][hapmap];0.80[ASN][1000 genomes]
rs9332113	0.85[CEU][hapmap];0.88[CHB][hapmap];0.80[ASN][1000 genomes]
rs9332116	0.92[YRI][hapmap];0.85[AFR][1000 genomes]
rs9332118	0.84[AFR][1000 genomes]
rs9332121	0.92[YRI][hapmap];0.88[AFR][1000 genomes]
rs9332127	0.85[AFR][1000 genomes]
rs9332128	0.92[YRI][hapmap];0.83[AFR][1000 genomes]
rs9332129	0.83[AFR][1000 genomes]
rs9332140	0.89[CHB][hapmap];0.80[ASN][1000 genomes]
rs9332167	0.80[ASN][1000 genomes]
rs9332198	0.92[YRI][hapmap];0.81[AFR][1000 genomes]
rs9783239	0.80[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv497859	chr10:96058024-97027747	Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	esv3380017	chr10:96439904-96662339	Enhancers ZNF genes & repeats Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	esv3344949	chr10:96443874-96666028	Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv551955	chr10:96444249-96690371	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1035409	chr10:96495177-96832057	Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
6	esv3529538	chr10:96522848-96700018	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	esv3529539	chr10:96522848-96700018	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	esv3361914	chr10:96522865-96700024	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv523259	chr10:96534584-96693727	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv1052578	chr10:96538082-96641949	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS	TF binding region lncRNA	3 gene(s)	inside rSNPs	diseases
11	esv3336672	chr10:96543010-96711519	Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv1037973	chr10:96563228-96711744	Weak transcription Active TSS Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	nsv1047782	chr10:96581094-96718479	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
14	esv1818389	chr10:96620304-96675513	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
15	nsv529726	chr10:96632494-97106315	Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2093434	CYP2C19	cis	Esophagus Mucosa	GTEx

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:96602800-96639400	Weak transcription	Gastric	stomach
2	chr10:96619200-96652200	Weak transcription	Duodenum Mucosa	Duodenum
3	chr10:96623000-96649600	Weak transcription	Fetal Intestine Large	intestine
4	chr10:96638800-96639000	Flanking Active TSS	Liver	Liver
5	chr10:96638800-96639200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr10:96638800-96639800	ZNF genes & repeats	Fetal Intestine Small	intestine

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