Variant report

Variant	rs12615975
Chromosome Location	chr2:231046438-231046439
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 86 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10168052	0.94[ASN][1000 genomes]
rs10177277	0.94[ASN][1000 genomes]
rs10755048	0.94[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs10755049	0.94[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs10755050	0.98[ASN][1000 genomes]
rs10804364	0.94[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs10933328	0.98[ASN][1000 genomes]
rs1124534	0.89[CHB][hapmap];0.96[CHD][hapmap];0.94[GIH][hapmap];0.92[JPT][hapmap];0.96[TSI][hapmap];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11556887	1.00[ASW][hapmap];0.89[CEU][hapmap];0.87[MKK][hapmap];0.88[TSI][hapmap];0.85[EUR][1000 genomes]
rs12474611	0.84[ASN][1000 genomes]
rs12474616	0.95[ASN][1000 genomes]
rs12474683	0.94[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs12616762	0.98[ASN][1000 genomes]
rs12618921	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12619729	0.94[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs12619732	0.94[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1469345	0.90[ASN][1000 genomes]
rs1896258	0.94[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs1896259	0.94[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs1978582	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1978583	0.94[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1985603	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2081714	0.95[ASN][1000 genomes]
rs2114592	0.80[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.96[TSI][hapmap];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2396709	0.94[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2396711	0.98[ASN][1000 genomes]
rs3769837	0.91[ASN][1000 genomes]
rs3769839	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs41309108	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs41345344	0.80[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.96[TSI][hapmap];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs41423848	0.80[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.96[TSI][hapmap];0.95[ASN][1000 genomes]
rs4327229	0.98[ASN][1000 genomes]
rs4327230	0.94[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs4972942	0.95[ASN][1000 genomes]
rs4973285	0.94[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs4973286	0.98[ASN][1000 genomes]
rs4973287	0.94[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs4973288	0.98[ASN][1000 genomes]
rs4973289	0.94[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs4973290	0.94[ASN][1000 genomes]
rs4973291	0.92[ASN][1000 genomes]
rs4973292	0.95[ASN][1000 genomes]
rs4973293	0.95[ASN][1000 genomes]
rs4973294	0.93[CHB][hapmap];0.89[JPT][hapmap];0.95[ASN][1000 genomes]
rs4973296	0.91[ASN][1000 genomes]
rs4973297	0.95[ASN][1000 genomes]
rs4973298	0.94[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs55809057	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55945652	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55956818	0.90[ASN][1000 genomes]
rs56159955	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56275915	0.94[ASN][1000 genomes]
rs56301614	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56412815	0.94[ASN][1000 genomes]
rs59536070	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61182521	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6436919	0.88[ASN][1000 genomes]
rs6735604	0.84[CHB][hapmap];0.88[ASN][1000 genomes]
rs6743028	0.95[ASN][1000 genomes]
rs67469122	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6750748	0.95[ASN][1000 genomes]
rs6752361	0.94[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs6755998	0.87[ASN][1000 genomes]
rs72982403	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72982411	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72982413	0.85[ASN][1000 genomes]
rs72982416	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72982421	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72982424	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73000348	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73000367	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73000371	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7561924	0.95[ASN][1000 genomes]
rs7583769	0.95[ASN][1000 genomes]
rs7592927	0.95[ASN][1000 genomes]
rs7603350	0.95[ASN][1000 genomes]
rs9061	0.88[EUR][1000 genomes]
rs930031	0.93[ASN][1000 genomes]
rs930032	0.94[CHB][hapmap];0.82[JPT][hapmap];0.94[ASN][1000 genomes]
rs958978	0.94[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007920	chr2:230775427-231065592	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv1001562	chr2:230862717-231187043	Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv536156	chr2:230862717-231187043	Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv498047	chr2:230951712-231250489	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv869834	chr2:231045013-231139827	Strong transcription Flanking Active TSS Weak transcription Genic enhancers Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv998291	chr2:231045388-231136278	Enhancers Weak transcription Genic enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:231028400-231067000	Strong transcription	Primary B cells from peripheral blood	blood
2	chr2:231028600-231051200	Strong transcription	Primary T helper cells fromperipheralblood	blood
3	chr2:231028800-231051600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr2:231030800-231051000	Strong transcription	Primary T cells fromperipheralblood	blood
5	chr2:231030800-231051000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr2:231031200-231049800	Weak transcription	HSMMtube	muscle
7	chr2:231031400-231051000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr2:231031400-231051000	Strong transcription	Fetal Thymus	thymus
9	chr2:231031400-231051600	Strong transcription	GM12878-XiMat	blood
10	chr2:231031400-231061200	Strong transcription	Primary B cells from cord blood	blood
11	chr2:231031600-231050800	Strong transcription	Fetal Muscle Leg	muscle
12	chr2:231031600-231052400	Weak transcription	Fetal Brain Male	brain
13	chr2:231031800-231049400	Strong transcription	Liver	Liver
14	chr2:231033800-231050800	Strong transcription	Dnd41	blood
15	chr2:231034800-231047400	Weak transcription	Small Intestine	intestine
16	chr2:231035000-231051800	Strong transcription	Primary T cells from cord blood	blood
17	chr2:231035400-231077000	Weak transcription	HepG2	liver
18	chr2:231035600-231049000	Weak transcription	Brain Angular Gyrus	brain
19	chr2:231035600-231050400	Strong transcription	Primary monocytes fromperipheralblood	blood
20	chr2:231035600-231050400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr2:231035600-231050800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr2:231035600-231050800	Strong transcription	Thymus	Thymus
23	chr2:231035600-231051000	Strong transcription	Primary neutrophils fromperipheralblood	blood
24	chr2:231035600-231051000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr2:231035600-231051200	Strong transcription	Monocytes-CD14+_RO01746	blood
26	chr2:231035600-231051600	Strong transcription	Primary T helper cells PMA-I stimulated	--
27	chr2:231035800-231049600	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr2:231035800-231062800	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr2:231036000-231048400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr2:231036200-231048800	Strong transcription	Lung	lung
31	chr2:231036200-231049200	Strong transcription	Adipose Nuclei	Adipose
32	chr2:231036200-231050800	Strong transcription	Duodenum Smooth Muscle	Duodenum
33	chr2:231036200-231051200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr2:231036400-231051200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr2:231036600-231048200	Strong transcription	Stomach Smooth Muscle	stomach
36	chr2:231036600-231048800	Strong transcription	Fetal Muscle Trunk	muscle
37	chr2:231036600-231051200	Strong transcription	Ovary	ovary
38	chr2:231036800-231051000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
39	chr2:231036800-231071800	Weak transcription	NHEK	skin
40	chr2:231036800-231073600	Weak transcription	HMEC	breast
41	chr2:231037000-231049000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr2:231037200-231049000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr2:231037200-231050800	Strong transcription	Spleen	Spleen
44	chr2:231037200-231051000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr2:231037400-231047200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
46	chr2:231037400-231049800	Strong transcription	Primary T helper naive cells from peripheral blood	blood
47	chr2:231038000-231069600	Weak transcription	NHLF	lung
48	chr2:231038800-231049200	Strong transcription	Duodenum Mucosa	Duodenum
49	chr2:231039000-231048200	Strong transcription	Left Ventricle	heart
50	chr2:231039000-231050800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland

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