Variant report

Variant	rs12632867
Chromosome Location	chr3:112202384-112202385
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 88 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs1386895	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.87[TSI][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1398091	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs1512006	0.82[CEU][hapmap];0.94[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap]
rs1533159	0.81[CHB][hapmap]
rs1814052	0.93[EUR][1000 genomes]
rs1844089	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs1873571	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap]
rs1873572	0.81[CHB][hapmap]
rs1877363	0.82[CEU][hapmap];0.94[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap]
rs2171513	0.82[CEU][hapmap];0.81[CHB][hapmap];1.00[TSI][hapmap]
rs2171514	0.90[EUR][1000 genomes]
rs2633555	0.97[ASN][1000 genomes]
rs2633556	0.90[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs2633557	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs2633560	0.93[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs2633562	0.82[ASW][hapmap];1.00[CEU][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs2633563	0.97[EUR][1000 genomes]
rs2633574	0.81[CHB][hapmap]
rs2633578	0.82[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.87[ASN][1000 genomes]
rs2633579	1.00[CEU][hapmap];0.81[CHB][hapmap];0.93[EUR][1000 genomes]
rs2633580	0.82[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.87[ASN][1000 genomes]
rs2633582	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs2633584	0.87[ASN][1000 genomes]
rs2633588	0.93[EUR][1000 genomes]
rs2633589	0.93[EUR][1000 genomes]
rs2638013	0.93[EUR][1000 genomes]
rs2638015	0.90[EUR][1000 genomes]
rs2638016	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs2638017	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs2638018	0.80[ASN][1000 genomes]
rs2638019	0.81[CHB][hapmap]
rs2638022	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap]
rs2638023	0.81[CHB][hapmap]
rs2638026	0.81[CHB][hapmap]
rs2638029	0.81[CHB][hapmap]
rs2638031	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap]
rs2638032	0.81[CHB][hapmap]
rs2638035	0.81[CHB][hapmap]
rs2638037	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs2638039	0.91[CHB][hapmap]
rs2705507	0.81[CHB][hapmap]
rs2705517	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2705521	0.81[CHB][hapmap]
rs2705522	0.81[CHB][hapmap]
rs2705525	0.93[EUR][1000 genomes]
rs2705531	0.97[ASN][1000 genomes]
rs2705532	0.96[ASN][1000 genomes]
rs2705533	0.93[EUR][1000 genomes]
rs2705534	0.82[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.96[ASN][1000 genomes]
rs2705536	0.93[EUR][1000 genomes]
rs2705541	0.81[CHB][hapmap]
rs2705544	1.00[CEU][hapmap];0.81[CHB][hapmap];1.00[TSI][hapmap];0.93[EUR][1000 genomes]
rs2705555	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs2705556	0.81[CHB][hapmap]
rs2705559	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2705562	0.81[CHB][hapmap]
rs2705565	1.00[CEU][hapmap];0.81[CHB][hapmap];0.93[EUR][1000 genomes]
rs2705566	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs2933134	0.81[CHB][hapmap]
rs2933135	0.81[CHB][hapmap]
rs2933142	0.80[ASN][1000 genomes]
rs2952319	0.81[CHB][hapmap]
rs2952323	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs2952326	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs2952327	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs2969896	0.81[CHB][hapmap]
rs2971204	1.00[CEU][hapmap];0.81[CHB][hapmap];0.93[EUR][1000 genomes]
rs4519670	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4682410	0.82[CEU][hapmap];0.94[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.87[TSI][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6438079	1.00[CEU][hapmap];0.94[CHB][hapmap];0.89[CHD][hapmap];0.94[JPT][hapmap];0.81[MEX][hapmap];0.87[TSI][hapmap];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6792947	0.82[CEU][hapmap];0.94[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap]
rs728568	0.81[CHB][hapmap]
rs7652377	0.82[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap]
rs766968	0.82[CEU][hapmap];0.94[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap]
rs9288952	0.82[CEU][hapmap];0.88[CHB][hapmap];0.86[CHD][hapmap];0.89[JPT][hapmap];0.87[TSI][hapmap]
rs9756562	0.87[ASN][1000 genomes]
rs9848054	0.82[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap]
rs9866734	0.82[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap]
rs9869455	1.00[CEU][hapmap];0.85[CHB][hapmap];0.93[JPT][hapmap]
rs9869579	1.00[CEU][hapmap];0.93[CHB][hapmap];0.86[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv591294	chr3:112091220-112208750	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1010208	chr3:112098542-112227212	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1003936	chr3:112125931-112274613	Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv998309	chr3:112130290-112278804	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
5	nsv591300	chr3:112144026-112270857	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
6	nsv1006065	chr3:112147080-112276983	Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
7	nsv1005323	chr3:112171990-112274613	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
8	nsv877342	chr3:112185025-112332629	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:112194200-112214000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr3:112197000-112203800	Genic enhancers	Primary B cells from peripheral blood	blood
3	chr3:112199200-112203600	Enhancers	Primary T helper cells fromperipheralblood	blood
4	chr3:112199800-112202600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
5	chr3:112199800-112202600	Enhancers	Primary T killer memory cells from peripheral blood	blood
6	chr3:112200000-112202400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr3:112200200-112202400	Enhancers	Primary T cells from cord blood	blood
8	chr3:112200200-112203800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr3:112200400-112214800	Weak transcription	Fetal Thymus	thymus
10	chr3:112200600-112203400	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr3:112200600-112208600	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr3:112200600-112217000	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr3:112201400-112208600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr3:112201400-112215600	Weak transcription	Duodenum Mucosa	Duodenum
15	chr3:112201600-112202600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr3:112201800-112202600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
17	chr3:112201800-112203600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
18	chr3:112201800-112208600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr3:112202200-112203800	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
20	chr3:112202200-112206800	Strong transcription	Primary B cells from cord blood	blood
21	chr3:112202200-112208600	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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