Variant report

Variant	rs10134592
Chromosome Location	chr14:67640666-67640667
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 125 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:118)

rs_ID	r²[population]
rs10129779	0.81[JPT][hapmap]
rs10131212	0.86[CHD][hapmap];0.82[JPT][hapmap]
rs10131984	0.92[ASN][1000 genomes]
rs10132088	0.94[ASN][1000 genomes]
rs10135903	0.82[JPT][hapmap]
rs10137557	0.85[JPT][hapmap]
rs10138824	0.86[CHD][hapmap];0.82[JPT][hapmap]
rs10138850	0.82[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];0.87[MEX][hapmap];0.89[MKK][hapmap];0.95[YRI][hapmap];0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10138865	0.82[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];0.94[YRI][hapmap];0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10139792	0.96[ASN][1000 genomes]
rs10140817	0.82[JPT][hapmap]
rs10141879	0.85[CHD][hapmap];0.90[JPT][hapmap]
rs10141952	0.81[ASN][1000 genomes]
rs10144090	0.86[CHD][hapmap];0.86[JPT][hapmap]
rs10144371	0.86[ASN][1000 genomes]
rs10144401	0.83[CHD][hapmap];0.82[JPT][hapmap]
rs10144417	0.83[CHD][hapmap];0.82[JPT][hapmap]
rs10145508	0.89[ASN][1000 genomes]
rs10145511	0.86[ASN][1000 genomes]
rs10145586	0.81[JPT][hapmap]
rs10146663	0.83[CHD][hapmap];0.82[JPT][hapmap]
rs10147852	0.86[CHD][hapmap];0.82[JPT][hapmap]
rs10150902	0.83[CHD][hapmap];0.82[JPT][hapmap]
rs10151464	0.82[JPT][hapmap]
rs10431718	0.86[CHD][hapmap];0.82[JPT][hapmap]
rs1045060	0.83[CHD][hapmap];0.86[JPT][hapmap]
rs10459453	0.82[JPT][hapmap]
rs10483793	0.81[ASN][1000 genomes]
rs1073607	0.82[JPT][hapmap]
rs1078194	0.91[JPT][hapmap]
rs10873200	0.82[JPT][hapmap]
rs11158655	0.86[CHD][hapmap];0.82[JPT][hapmap]
rs12323494	0.81[JPT][hapmap]
rs12323911	0.83[CHD][hapmap];0.82[JPT][hapmap]
rs12588458	0.82[MEX][hapmap]
rs12588478	0.81[JPT][hapmap]
rs12589218	0.82[JPT][hapmap]
rs12589671	0.82[JPT][hapmap]
rs12590689	0.83[ASN][1000 genomes]
rs12590956	0.91[JPT][hapmap]
rs1318914	0.82[JPT][hapmap]
rs13379142	0.80[JPT][hapmap]
rs13379368	0.82[JPT][hapmap]
rs1535491	0.86[CHD][hapmap];0.82[JPT][hapmap]
rs1536271	0.82[JPT][hapmap]
rs1536272	0.82[JPT][hapmap]
rs17104103	0.83[CHD][hapmap];0.82[JPT][hapmap]
rs17104106	0.82[JPT][hapmap]
rs17104109	0.82[JPT][hapmap]
rs17104114	0.81[CHD][hapmap];0.91[JPT][hapmap]
rs17248252	0.87[ASN][1000 genomes]
rs17248357	0.95[ASN][1000 genomes]
rs17248421	1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[JPT][hapmap];0.89[LWK][hapmap];0.81[YRI][hapmap];0.97[ASN][1000 genomes]
rs17248526	0.86[CHD][hapmap];0.82[JPT][hapmap]
rs17248616	0.80[JPT][hapmap]
rs1885589	0.81[JPT][hapmap]
rs1918483	0.82[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];0.87[MEX][hapmap];0.89[MKK][hapmap];0.95[YRI][hapmap];0.88[AFR][1000 genomes];0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1952337	0.83[CHB][hapmap];0.83[JPT][hapmap]
rs2031563	0.83[CHD][hapmap]
rs2039055	0.84[ASN][1000 genomes]
rs2057396	0.82[JPT][hapmap]
rs2146229	0.86[CHD][hapmap];0.82[JPT][hapmap]
rs2146230	0.86[CHD][hapmap];0.82[JPT][hapmap]
rs2236333	0.82[JPT][hapmap]
rs2274335	0.82[JPT][hapmap]
rs2274338	0.82[JPT][hapmap]
rs2281676	0.91[ASN][1000 genomes]
rs2295903	0.97[ASN][1000 genomes]
rs28368552	0.96[ASN][1000 genomes]
rs3752993	0.95[CHB][hapmap];0.93[CHD][hapmap];0.80[GIH][hapmap];0.91[JPT][hapmap]
rs3759755	0.83[CHD][hapmap];0.82[JPT][hapmap]
rs3818467	0.83[CHD][hapmap];0.82[JPT][hapmap]
rs3866760	1.00[CHB][hapmap];0.95[CHD][hapmap];0.91[JPT][hapmap];0.90[ASN][1000 genomes]
rs58221168	0.85[ASN][1000 genomes]
rs6573752	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.88[ASN][1000 genomes]
rs6573754	0.82[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs6573755	1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[JPT][hapmap];0.89[LWK][hapmap];0.81[YRI][hapmap];0.97[ASN][1000 genomes]
rs6573760	0.83[CHD][hapmap];0.91[JPT][hapmap]
rs6573763	0.89[JPT][hapmap]
rs7141519	0.95[CHB][hapmap];0.93[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap]
rs7146638	1.00[CHB][hapmap];0.95[CHD][hapmap];0.91[JPT][hapmap];0.81[LWK][hapmap];0.88[ASN][1000 genomes]
rs7147207	0.90[ASN][1000 genomes]
rs7147534	0.89[ASN][1000 genomes]
rs7148044	0.99[ASN][1000 genomes]
rs7148425	0.99[ASN][1000 genomes]
rs7149535	0.82[JPT][hapmap]
rs7150089	0.95[ASN][1000 genomes]
rs7150934	0.94[ASN][1000 genomes]
rs7151898	0.91[ASN][1000 genomes]
rs7152217	0.97[ASN][1000 genomes]
rs7152231	0.88[ASN][1000 genomes]
rs7152903	0.86[CHD][hapmap];0.81[JPT][hapmap]
rs7154905	0.90[ASN][1000 genomes]
rs7156119	0.88[AFR][1000 genomes];0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs7156441	0.83[CHD][hapmap];0.86[JPT][hapmap]
rs7157394	0.87[ASN][1000 genomes]
rs7157418	0.86[ASN][1000 genomes]
rs7158228	0.87[ASN][1000 genomes]
rs7161664	0.95[CHB][hapmap];0.93[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap]
rs7493580	0.84[ASN][1000 genomes]
rs8004148	0.83[CHD][hapmap];0.90[JPT][hapmap]
rs8004488	0.81[CHD][hapmap];0.91[JPT][hapmap]
rs8005981	0.92[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs8006281	0.95[ASN][1000 genomes]
rs8006391	0.81[JPT][hapmap]
rs8006519	0.83[CHD][hapmap]
rs8008236	0.82[JPT][hapmap]
rs8008619	0.85[CHD][hapmap];0.82[JPT][hapmap]
rs8009087	0.80[ASN][1000 genomes]
rs8009318	0.82[JPT][hapmap]
rs8010261	1.00[CHB][hapmap];0.95[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.89[ASN][1000 genomes]
rs8014966	0.82[JPT][hapmap]
rs8015862	0.82[JPT][hapmap]
rs8016037	0.86[CHD][hapmap];0.82[JPT][hapmap]
rs8019510	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs8021896	0.86[CHD][hapmap];0.82[JPT][hapmap]
rs9323494	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9743911	0.82[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv902058	chr14:67310195-67760538	Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv902059	chr14:67352226-67760538	ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
3	esv2751285	chr14:67364747-67886781	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
4	nsv902060	chr14:67417083-67760538	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	nsv1045518	chr14:67529049-67959582	Strong transcription Bivalent Enhancer Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
6	nsv832821	chr14:67590418-67828169	Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	nsv1040257	chr14:67634585-67762806	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10134592	EIF2S1	cis	multi-tissue	Pritchard

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:67600800-67647400	Weak transcription	Fetal Kidney	kidney
2	chr14:67614400-67653200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr14:67618400-67658200	Weak transcription	Brain Angular Gyrus	brain
4	chr14:67630000-67645600	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr14:67631600-67645800	Weak transcription	Psoas Muscle	Psoas
6	chr14:67633200-67645400	Weak transcription	Rectal Smooth Muscle	rectum
7	chr14:67634600-67653200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr14:67635000-67652800	Weak transcription	NHEK	skin
9	chr14:67635000-67653200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr14:67635200-67645200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr14:67636200-67645400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr14:67638000-67645400	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr14:67639400-67646200	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr14:67639600-67647400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr14:67639600-67647400	Weak transcription	Right Ventricle	heart
16	chr14:67639600-67658600	Weak transcription	Stomach Smooth Muscle	stomach
17	chr14:67639800-67647400	Weak transcription	Gastric	stomach
18	chr14:67640000-67641800	Weak transcription	Brain Cingulate Gyrus	brain
19	chr14:67640000-67643800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr14:67640000-67647000	Weak transcription	Pancreas	Pancrea
21	chr14:67640200-67640800	Weak transcription	Fetal Brain Male	brain
22	chr14:67640200-67645800	Weak transcription	Fetal Stomach	stomach
23	chr14:67640200-67646000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr14:67640200-67649600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr14:67640400-67641200	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr14:67640400-67645200	Weak transcription	Colon Smooth Muscle	Colon
27	chr14:67640400-67645400	Weak transcription	Brain Hippocampus Middle	brain
28	chr14:67640400-67645600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr14:67640400-67645600	Weak transcription	Aorta	Aorta
30	chr14:67640400-67645600	Weak transcription	Duodenum Mucosa	Duodenum
31	chr14:67640400-67645600	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr14:67640400-67646200	Weak transcription	Ovary	ovary
33	chr14:67640400-67646800	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr14:67640400-67647400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr14:67640600-67646800	Weak transcription	Rectal Mucosa Donor 29	rectum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links