Variant report

Variant	rs10774466
Chromosome Location	chr12:939302-939303
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 100 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs1012729	0.95[CEU][hapmap];0.88[GIH][hapmap];0.95[MEX][hapmap];0.91[TSI][hapmap];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1051669	0.95[CEU][hapmap];0.81[GIH][hapmap];0.91[TSI][hapmap];0.81[EUR][1000 genomes]
rs1051672	0.80[EUR][1000 genomes]
rs10735063	0.81[ASN][1000 genomes]
rs10735065	1.00[ASN][1000 genomes]
rs10774459	0.81[ASN][1000 genomes]
rs10774463	0.93[ASN][1000 genomes]
rs10774464	0.86[JPT][hapmap]
rs10774468	0.90[CEU][hapmap];0.83[AMR][1000 genomes]
rs10849559	0.86[JPT][hapmap]
rs10849561	0.87[AFR][1000 genomes]
rs10849562	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10849563	1.00[CHB][hapmap];0.95[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10849568	1.00[ASN][1000 genomes]
rs10849583	0.81[EUR][1000 genomes]
rs11064519	0.82[JPT][hapmap]
rs11064560	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11064582	0.81[EUR][1000 genomes]
rs11064584	0.95[CEU][hapmap];0.81[EUR][1000 genomes]
rs11513723	0.81[EUR][1000 genomes]
rs11571430	0.90[CEU][hapmap];0.88[GIH][hapmap];0.95[MEX][hapmap];0.91[TSI][hapmap]
rs1159744	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11608756	0.86[JPT][hapmap]
rs11829138	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11832907	0.95[CEU][hapmap];0.85[YRI][hapmap];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1970996	1.00[ASN][1000 genomes]
rs1990021	0.97[ASN][1000 genomes]
rs2014160	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2051852	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2107612	1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs2107613	0.85[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs2107614	0.93[ASN][1000 genomes]
rs2158502	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2240282	1.00[ASN][1000 genomes]
rs2240283	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2286007	0.85[CHB][hapmap];0.85[JPT][hapmap]
rs2301880	1.00[CEU][hapmap];0.95[MEX][hapmap];0.88[TSI][hapmap];0.83[EUR][1000 genomes]
rs2369402	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2369490	0.90[ASN][1000 genomes]
rs2369491	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3858703	0.86[CHB][hapmap];0.85[JPT][hapmap]
rs4388955	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4390400	0.86[AMR][1000 genomes]
rs4766377	0.95[CEU][hapmap];0.95[MEX][hapmap];0.88[TSI][hapmap]
rs4980969	1.00[ASN][1000 genomes]
rs4980970	1.00[ASN][1000 genomes]
rs4980972	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6489746	0.80[CEU][hapmap];0.86[CHB][hapmap];0.85[JPT][hapmap]
rs6489749	0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6489751	0.97[ASN][1000 genomes]
rs6489752	1.00[CEU][hapmap];0.96[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6489754	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6489757	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67969314	0.96[ASN][1000 genomes]
rs724709	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7298001	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7300056	1.00[ASN][1000 genomes]
rs7301349	1.00[ASN][1000 genomes]
rs7309858	0.97[ASN][1000 genomes]
rs7311065	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7311423	1.00[ASN][1000 genomes]
rs765250	1.00[CHB][hapmap];0.95[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs7953912	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7959921	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7966632	0.93[ASN][1000 genomes]
rs7971329	1.00[ASN][1000 genomes]
rs7972490	1.00[CEU][hapmap];0.95[MEX][hapmap];0.91[TSI][hapmap];0.81[EUR][1000 genomes]
rs7972667	0.86[CHB][hapmap];0.85[JPT][hapmap]
rs7980163	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:31 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv541305	chr12:282465-1016828	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
2	nsv869390	chr12:282465-1045994	Strong transcription Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
3	nsv1049944	chr12:282465-1232077	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
4	nsv541306	chr12:282465-1232077	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic 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	80 gene(s)	inside rSNPs	diseases
5	nsv1044433	chr12:321619-1065402	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
6	nsv541323	chr12:321619-1065402	Strong transcription Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
7	esv2759875	chr12:335010-990544	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
8	nsv949469	chr12:380411-1122450	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
9	esv2758290	chr12:457433-990544	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
10	nsv898568	chr12:547683-969800	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
11	nsv556890	chr12:662448-1100555	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
12	nsv556892	chr12:673515-1210884	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
13	nsv1051590	chr12:722215-974773	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
14	nsv541338	chr12:722215-974773	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
15	nsv468956	chr12:737230-982321	Strong transcription Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
16	nsv556893	chr12:737230-982321	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
17	esv2757485	chr12:786238-964551	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
18	nsv898576	chr12:813411-1553450	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
19	esv2753750	chr12:835074-939480	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
20	esv2753658	chr12:835074-964506	Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
21	esv3693103	chr12:837113-971317	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS 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	22 gene(s)	inside rSNPs	diseases
22	nsv556898	chr12:850288-968489	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
23	nsv518946	chr12:854331-961336	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
24	nsv556900	chr12:854331-968489	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
25	esv2752382	chr12:863833-964506	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
26	nsv948760	chr12:863833-1542875	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
27	nsv898577	chr12:873890-969800	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
28	nsv1042333	chr12:907975-1081509	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
29	nsv1052589	chr12:910460-1421493	ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
30	nsv1045278	chr12:920251-1697030	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
31	nsv522901	chr12:922408-968489	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs10774466	WNK1	cis	parietal	SCAN
rs10774466	RAD52	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:905400-957000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:905400-970200	Weak transcription	Spleen	Spleen
3	chr12:914400-971000	Weak transcription	Right Ventricle	heart
4	chr12:916400-977200	Weak transcription	Gastric	stomach
5	chr12:916800-955800	Weak transcription	Stomach Mucosa	stomach
6	chr12:920200-947200	Weak transcription	Small Intestine	intestine
7	chr12:920200-966800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr12:921400-950200	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr12:922200-940800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr12:928000-960600	Weak transcription	Aorta	Aorta
11	chr12:928200-994400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr12:932800-954800	Weak transcription	Fetal Kidney	kidney
13	chr12:933400-952200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr12:933600-942800	Strong transcription	HepG2	liver
15	chr12:933600-966600	Weak transcription	Fetal Brain Female	brain
16	chr12:933600-971400	Weak transcription	Fetal Brain Male	brain
17	chr12:934000-944200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr12:934200-940600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr12:934600-970200	Weak transcription	Colonic Mucosa	Colon
20	chr12:935000-940800	Strong transcription	HUES64 Cell Line	embryonic stem cell
21	chr12:935000-940800	Strong transcription	Fetal Thymus	thymus
22	chr12:935000-943800	Strong transcription	Placenta	Placenta
23	chr12:935200-940200	Strong transcription	HMEC	breast
24	chr12:935200-940600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr12:935200-940800	Strong transcription	HUES48 Cell Line	embryonic stem cell
26	chr12:935200-941200	Strong transcription	GM12878-XiMat	blood
27	chr12:935200-942600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr12:935200-944200	Strong transcription	Monocytes-CD14+_RO01746	blood
29	chr12:935200-944600	Strong transcription	Dnd41	blood
30	chr12:935200-945000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr12:935400-940200	Strong transcription	NH-A	brain
32	chr12:935400-940600	Strong transcription	HUES6 Cell Line	embryonic stem cell
33	chr12:935400-940800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr12:935800-940400	Strong transcription	A549	lung
35	chr12:935800-940600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
36	chr12:935800-943800	Strong transcription	Primary B cells from cord blood	blood
37	chr12:935800-944400	Weak transcription	Fetal Heart	heart
38	chr12:936000-939600	Strong transcription	Fetal Intestine Large	intestine
39	chr12:936000-939800	Strong transcription	Rectal Mucosa Donor 29	rectum
40	chr12:936000-940200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
41	chr12:936000-940400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
42	chr12:936000-944000	Strong transcription	HSMM	muscle
43	chr12:936000-945000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr12:936000-948200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr12:936200-939600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr12:936200-939600	Strong transcription	Thymus	Thymus
47	chr12:936200-939600	Strong transcription	NHLF	lung
48	chr12:936200-940400	Strong transcription	Primary T helper naive cells from peripheral blood	blood
49	chr12:936200-940400	Strong transcription	Duodenum Smooth Muscle	Duodenum
50	chr12:936200-940400	Strong transcription	Osteobl	bone

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