Variant report

Variant	rs12768009
Chromosome Location	chr10:96525865-96525866
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 149 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:116)

rs_ID	r²[population]
rs1042192	1.00[CEU][hapmap];0.82[CHD][hapmap];0.97[GIH][hapmap];0.80[JPT][hapmap];0.82[LWK][hapmap];0.93[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1042194	1.00[CEU][hapmap];0.83[CHB][hapmap];0.82[CHD][hapmap];0.97[GIH][hapmap];0.80[JPT][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10509676	1.00[CEU][hapmap];0.83[CHB][hapmap];0.80[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10509679	0.84[GIH][hapmap];0.92[MEX][hapmap];0.84[TSI][hapmap]
rs1074145	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12569735	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12569873	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12570771	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12570829	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12571421	1.00[ASW][hapmap];1.00[CEU][hapmap];0.83[CHB][hapmap];0.97[GIH][hapmap];0.80[JPT][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12571533	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12572085	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12572351	0.84[GIH][hapmap];0.92[MEX][hapmap];0.84[TSI][hapmap]
rs12572499	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12572917	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12573074	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12762136	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12762370	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12763230	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12767583	1.00[ASW][hapmap];0.92[CEU][hapmap];0.84[CHD][hapmap];0.97[GIH][hapmap];0.80[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12769205	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12772672	1.00[CEU][hapmap];0.83[CHB][hapmap];0.81[CHD][hapmap];0.97[GIH][hapmap];0.80[JPT][hapmap];0.85[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.81[YRI][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12773342	1.00[CEU][hapmap];0.83[CHB][hapmap];0.80[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs12773527	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12773884	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12774450	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12774901	0.85[GIH][hapmap];0.86[YRI][hapmap]
rs12775283	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12775423	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12775707	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12777311	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12777823	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12778026	1.00[CEU][hapmap];0.83[CHB][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12778216	0.88[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12778966	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12781477	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12782132	0.84[CEU][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12783509	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12783988	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12784219	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12784245	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12785038	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1322179	1.00[ASW][hapmap];1.00[CEU][hapmap];0.83[CHB][hapmap];0.82[CHD][hapmap];0.97[GIH][hapmap];0.80[JPT][hapmap];0.81[LWK][hapmap];0.92[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1326832	1.00[CEU][hapmap];0.83[CHB][hapmap];0.80[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1853205	1.00[CEU][hapmap];0.83[CHB][hapmap];0.80[JPT][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1926711	0.89[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.94[TSI][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1926712	1.00[CEU][hapmap];0.83[CHB][hapmap];0.81[CHD][hapmap];0.97[GIH][hapmap];0.80[JPT][hapmap];0.85[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.81[YRI][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2025445	0.82[CHD][hapmap];0.84[LWK][hapmap];0.86[YRI][hapmap]
rs2093434	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2181097	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2281890	1.00[CEU][hapmap];0.83[CHB][hapmap];0.82[CHD][hapmap];0.97[GIH][hapmap];0.80[JPT][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2281891	1.00[ASW][hapmap];1.00[CEU][hapmap];0.82[CHD][hapmap];0.97[GIH][hapmap];0.80[JPT][hapmap];0.81[LWK][hapmap];0.93[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs2296680	1.00[CEU][hapmap];0.83[CHB][hapmap];0.82[CHD][hapmap];0.97[GIH][hapmap];0.80[JPT][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.81[YRI][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs28399513	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2860837	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2860838	1.00[CEU][hapmap];0.83[CHB][hapmap];0.82[CHD][hapmap];0.97[GIH][hapmap];0.80[JPT][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2860903	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs34058919	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34121168	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs34582766	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34607361	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs34777815	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs34829812	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35037138	0.90[AMR][1000 genomes]
rs35059536	0.83[EUR][1000 genomes]
rs35172334	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs35390752	1.00[CEU][hapmap];0.83[CHB][hapmap];0.97[GIH][hapmap];0.80[JPT][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.81[YRI][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs35391887	0.84[AMR][1000 genomes]
rs35709381	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35751085	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs35835168	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3758580	1.00[CEU][hapmap];0.83[CHB][hapmap];0.80[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs3818504	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4244285	1.00[CEU][hapmap];0.83[CHB][hapmap];0.80[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4255471	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4362080	0.82[ASN][1000 genomes]
rs4417205	1.00[CEU][hapmap];0.83[CHB][hapmap];0.80[JPT][hapmap];0.81[YRI][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4445573	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4532967	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4589212	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4641393	1.00[ASW][hapmap];1.00[CEU][hapmap];0.83[CHB][hapmap];0.82[CHD][hapmap];0.97[GIH][hapmap];0.80[JPT][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4986894	1.00[ASW][hapmap];1.00[CEU][hapmap];0.83[CHB][hapmap];0.97[GIH][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56229007	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs58335703	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs58447435	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6583954	1.00[CEU][hapmap];0.83[CHB][hapmap];0.82[CHD][hapmap];0.97[GIH][hapmap];0.80[JPT][hapmap];0.85[LWK][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.81[YRI][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs67120915	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs67482845	0.82[ASN][1000 genomes]
rs67941743	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7085420	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7085563	0.82[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7085890	1.00[CEU][hapmap];0.83[CHB][hapmap];0.80[JPT][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7089349	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7100783	1.00[CEU][hapmap];0.83[CHB][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs71482318	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs71482322	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs717238	1.00[CEU][hapmap];0.83[CHB][hapmap];0.82[CHD][hapmap];0.97[GIH][hapmap];0.80[JPT][hapmap];0.85[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.81[YRI][hapmap];0.91[EUR][1000 genomes]
rs72816638	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72816654	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72818619	0.83[EUR][1000 genomes]
rs7475739	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs749745	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7893282	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7900135	1.00[CEU][hapmap];0.83[CHB][hapmap];0.82[CHD][hapmap];0.97[GIH][hapmap];0.80[JPT][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7904581	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7907226	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7911008	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7911654	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7919524	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs932809	1.00[CEU][hapmap];0.83[CHB][hapmap];0.82[CHD][hapmap];0.97[GIH][hapmap];0.80[JPT][hapmap];0.85[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.81[YRI][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9332105	0.84[GIH][hapmap];0.92[MEX][hapmap];0.84[TSI][hapmap]
rs9332113	0.84[GIH][hapmap];0.92[MEX][hapmap];0.84[TSI][hapmap]
rs9332116	0.87[ASW][hapmap];0.81[LWK][hapmap];1.00[YRI][hapmap]
rs9332121	0.91[YRI][hapmap]
rs9332128	0.87[ASW][hapmap];0.81[LWK][hapmap];1.00[YRI][hapmap]
rs9783239	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:33 , 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	nsv934280	chr10:96401297-96540495	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv522538	chr10:96405329-96547463	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	nsv1047944	chr10:96407825-96563288	Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv1050653	chr10:96407825-96634161	Active TSS Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv1037364	chr10:96435433-96634161	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS 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
7	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
8	nsv1046308	chr10:96441300-96633012	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	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
10	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
11	nsv551956	chr10:96446632-96632253	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv534171	chr10:96453830-96612764	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
13	nsv551957	chr10:96454156-96626682	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	nsv1047505	chr10:96468200-96593083	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
15	nsv540748	chr10:96468200-96593083	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
16	nsv895901	chr10:96486504-96565650	Active TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
17	nsv1044621	chr10:96495177-96546535	Strong transcription ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
18	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
19	esv2761617	chr10:96495189-96548785	Strong transcription Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
20	nsv551958	chr10:96495793-96548132	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
21	nsv869918	chr10:96496856-96575687	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
22	nsv1049558	chr10:96497884-96558711	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
23	nsv1046919	chr10:96497884-96559165	Genic enhancers Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
24	nsv1039270	chr10:96497884-96565616	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
25	nsv551959	chr10:96499710-96557336	Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
26	esv2830208	chr10:96500106-96547463	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Genic enhancers	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
27	nsv551960	chr10:96500106-96547463	Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
28	nsv551961	chr10:96500106-96548132	Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
29	nsv895902	chr10:96500106-96619025	ZNF genes & repeats Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
30	esv2829935	chr10:96521249-96547463	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
31	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
32	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
33	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

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs12768009	CYP2C19	cis	Esophagus Mucosa	GTEx
rs12768009	PDE6C	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:96521800-96526000	Active TSS	Liver	Liver
2	chr10:96525600-96539400	Weak transcription	Duodenum Mucosa	Duodenum

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