Variant report

Variant	rs4964331
Chromosome Location	chr12:105476128-105476129
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 116 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:113)

rs_ID	r²[population]
rs10746010	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10778367	1.00[CEU][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10778368	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10778369	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11112434	0.85[CEU][hapmap]
rs1196742	0.87[EUR][1000 genomes]
rs1196745	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs1196748	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs1196749	1.00[CEU][hapmap];0.85[GIH][hapmap];0.87[TSI][hapmap];0.87[EUR][1000 genomes]
rs1196753	1.00[CEU][hapmap];0.85[GIH][hapmap];0.84[TSI][hapmap];0.83[EUR][1000 genomes]
rs1196754	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs1196756	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs1196764	0.87[EUR][1000 genomes]
rs1196765	0.86[EUR][1000 genomes]
rs1196770	0.81[EUR][1000 genomes]
rs1196772	0.81[EUR][1000 genomes]
rs1196777	0.80[EUR][1000 genomes]
rs1196780	0.85[CEU][hapmap]
rs1196795	0.85[CEU][hapmap];0.85[CHB][hapmap];0.83[CHD][hapmap]
rs1196797	0.85[CEU][hapmap];0.85[CHB][hapmap];0.83[CHD][hapmap]
rs1196798	1.00[CEU][hapmap];0.82[CHB][hapmap];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1196800	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs1196801	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs1196805	0.88[EUR][1000 genomes]
rs1196806	1.00[CEU][hapmap];0.85[GIH][hapmap];0.82[MEX][hapmap];0.91[TSI][hapmap];0.88[EUR][1000 genomes]
rs1196807	0.88[EUR][1000 genomes]
rs1196808	0.87[EUR][1000 genomes]
rs1196811	1.00[CEU][hapmap];0.82[CHB][hapmap];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1196813	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs1196817	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs1196819	1.00[CEU][hapmap];0.85[GIH][hapmap];0.82[MEX][hapmap];0.91[TSI][hapmap];0.88[EUR][1000 genomes]
rs1196820	0.88[EUR][1000 genomes]
rs1196823	0.87[EUR][1000 genomes]
rs1196825	0.88[EUR][1000 genomes]
rs1196831	0.88[EUR][1000 genomes]
rs1196833	0.88[EUR][1000 genomes]
rs1196839	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs1196841	0.88[EUR][1000 genomes]
rs1196842	1.00[CEU][hapmap];0.85[GIH][hapmap];0.91[TSI][hapmap];0.88[EUR][1000 genomes]
rs1196844	0.88[EUR][1000 genomes]
rs1196848	1.00[CEU][hapmap];0.85[GIH][hapmap];0.88[EUR][1000 genomes]
rs1196851	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs1196853	0.87[EUR][1000 genomes]
rs1196859	0.90[EUR][1000 genomes]
rs1196861	1.00[CEU][hapmap];0.85[GIH][hapmap];0.82[MEX][hapmap];0.87[TSI][hapmap];0.87[EUR][1000 genomes]
rs1196862	1.00[CEU][hapmap];0.85[GIH][hapmap];0.82[MEX][hapmap];0.91[TSI][hapmap];0.88[EUR][1000 genomes]
rs1196864	1.00[CEU][hapmap];0.85[GIH][hapmap];0.82[MEX][hapmap];0.87[TSI][hapmap];0.87[EUR][1000 genomes]
rs1196869	1.00[CEU][hapmap];0.85[GIH][hapmap];0.82[MEX][hapmap];0.87[TSI][hapmap];0.87[EUR][1000 genomes]
rs1196871	0.86[EUR][1000 genomes]
rs1196872	0.92[CEU][hapmap];0.85[GIH][hapmap];0.82[MEX][hapmap];0.87[TSI][hapmap];0.88[EUR][1000 genomes]
rs1196873	1.00[CEU][hapmap];0.85[GIH][hapmap];0.82[MEX][hapmap];0.87[TSI][hapmap];0.87[EUR][1000 genomes]
rs1196874	0.88[EUR][1000 genomes]
rs1196881	0.92[CEU][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1196884	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1196885	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1206559	0.88[EUR][1000 genomes]
rs1209308	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1209637	0.85[CEU][hapmap]
rs1211276	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs1211277	0.88[EUR][1000 genomes]
rs1345096	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1621553	0.92[CEU][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1663565	0.87[EUR][1000 genomes]
rs17036705	0.91[CHD][hapmap]
rs1732370	0.88[EUR][1000 genomes]
rs2166142	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2246243	0.80[EUR][1000 genomes]
rs2257156	1.00[CEU][hapmap];0.85[GIH][hapmap];0.82[MEX][hapmap];0.84[TSI][hapmap];0.87[EUR][1000 genomes]
rs2272491	0.91[CHD][hapmap]
rs2272494	0.81[ASN][1000 genomes]
rs2289773	0.91[CHD][hapmap]
rs2293642	0.91[CHD][hapmap]
rs2305047	0.81[ASN][1000 genomes]
rs2374449	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.96[TSI][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2440692	0.86[EUR][1000 genomes]
rs2440714	0.89[EUR][1000 genomes]
rs2440715	0.83[CEU][hapmap]
rs2440718	0.88[EUR][1000 genomes]
rs2464173	0.88[EUR][1000 genomes]
rs2464175	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs2464181	0.88[EUR][1000 genomes]
rs2464182	0.86[EUR][1000 genomes]
rs3794235	0.84[JPT][hapmap]
rs4356312	0.87[EUR][1000 genomes]
rs4356313	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4372534	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4390426	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4964122	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6539183	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6539186	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6539187	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6539188	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6539190	0.98[ASN][1000 genomes]
rs6539193	0.98[ASN][1000 genomes]
rs7132040	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7132624	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7132855	1.00[CEU][hapmap];0.86[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs71441895	0.81[EUR][1000 genomes]
rs7299166	1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs7299701	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7302854	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7303961	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7313896	0.86[JPT][hapmap]
rs73395721	0.93[ASN][1000 genomes]
rs7963877	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7973422	0.91[ASN][1000 genomes]
rs935240	1.00[CEU][hapmap];0.85[GIH][hapmap];0.82[MEX][hapmap];0.91[TSI][hapmap];0.88[EUR][1000 genomes]
rs935241	1.00[CEU][hapmap];0.85[GIH][hapmap];0.82[MEX][hapmap];0.91[TSI][hapmap];0.88[EUR][1000 genomes]
rs935242	0.88[EUR][1000 genomes]
rs935244	0.85[CEU][hapmap];0.81[EUR][1000 genomes]
rs935246	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs935248	0.87[EUR][1000 genomes]
rs935249	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899495	chr12:104990469-105527011	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv832505	chr12:105315352-105497765	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv832506	chr12:105461274-105637561	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs4964331	ALDH1L2	cis	cerebellum	SCAN
rs4964331	APPL2	cis	cerebellum	SCAN
rs4964331	ALDH1L2	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:105413000-105476800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:105420000-105477000	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr12:105441200-105477000	Weak transcription	Gastric	stomach
4	chr12:105447200-105477200	Weak transcription	Brain Hippocampus Middle	brain
5	chr12:105449400-105476800	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr12:105453400-105476800	Weak transcription	Rectal Smooth Muscle	rectum
7	chr12:105454200-105476600	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr12:105455600-105476400	Weak transcription	Fetal Brain Male	brain
9	chr12:105456000-105477000	Weak transcription	Brain Cingulate Gyrus	brain
10	chr12:105456800-105476800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr12:105460400-105476600	Weak transcription	Adipose Nuclei	Adipose
12	chr12:105460400-105476600	Weak transcription	Fetal Brain Female	brain
13	chr12:105460600-105476600	Weak transcription	Brain Germinal Matrix	brain
14	chr12:105464400-105476600	Weak transcription	Stomach Smooth Muscle	stomach
15	chr12:105464600-105476200	Weak transcription	NHLF	lung
16	chr12:105464600-105477000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr12:105464600-105477000	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr12:105465200-105476400	Weak transcription	NHDF-Ad	bronchial
19	chr12:105465400-105476800	Weak transcription	Fetal Muscle Leg	muscle
20	chr12:105467400-105476800	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr12:105467800-105476600	Weak transcription	NH-A	brain
22	chr12:105467800-105476800	Weak transcription	Fetal Stomach	stomach
23	chr12:105467800-105477000	Weak transcription	Brain Angular Gyrus	brain
24	chr12:105467800-105477000	Weak transcription	Fetal Muscle Trunk	muscle
25	chr12:105468000-105476200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr12:105470400-105476200	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr12:105470400-105476400	Weak transcription	HSMM	muscle
28	chr12:105470400-105476600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr12:105470600-105476800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr12:105470800-105476600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr12:105471000-105476200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr12:105471000-105477400	Weak transcription	Aorta	Aorta
33	chr12:105471800-105476200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr12:105471800-105476400	Weak transcription	HSMMtube	muscle
35	chr12:105473000-105476800	Weak transcription	Pancreas	Pancrea
36	chr12:105475000-105476800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr12:105475000-105478000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr12:105475200-105476600	Enhancers	K562	blood
39	chr12:105475400-105476600	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr12:105475400-105476600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr12:105475800-105476800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr12:105476000-105476200	Enhancers	Osteobl	bone
43	chr12:105476000-105476400	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr12:105476000-105477000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr12:105476000-105477200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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