Variant report

Variant	rs7154905
Chromosome Location	chr14:67639893-67639894
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 128 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:121)

rs_ID	r²[population]
rs10129779	0.90[JPT][hapmap]
rs10131212	0.88[CHD][hapmap];0.91[JPT][hapmap]
rs10131984	0.96[ASN][1000 genomes]
rs10132088	0.82[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs10134592	0.90[ASN][1000 genomes]
rs10135903	0.91[JPT][hapmap]
rs10137557	0.90[JPT][hapmap]
rs10138755	0.89[JPT][hapmap]
rs10138824	0.88[CHD][hapmap];0.91[JPT][hapmap]
rs10138850	1.00[CHB][hapmap];0.95[CHD][hapmap];0.91[JPT][hapmap];0.82[YRI][hapmap];0.86[ASN][1000 genomes]
rs10138865	1.00[CHB][hapmap];0.95[CHD][hapmap];0.90[JPT][hapmap];0.81[YRI][hapmap];0.86[ASN][1000 genomes]
rs10139792	0.87[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs10140817	0.91[JPT][hapmap]
rs10141879	0.87[CHD][hapmap];0.81[JPT][hapmap]
rs10141952	0.89[ASN][1000 genomes]
rs10144090	0.88[CHD][hapmap];0.90[JPT][hapmap]
rs10144371	0.94[ASN][1000 genomes]
rs10144401	0.85[CHD][hapmap];0.91[JPT][hapmap]
rs10144417	0.85[CHD][hapmap];0.91[JPT][hapmap]
rs10145508	0.92[ASN][1000 genomes]
rs10145511	0.90[ASN][1000 genomes]
rs10145586	0.90[JPT][hapmap]
rs10146663	0.85[CHD][hapmap];0.91[JPT][hapmap]
rs10146722	0.89[JPT][hapmap]
rs10147852	0.88[CHD][hapmap];0.91[JPT][hapmap]
rs10150902	0.85[CHD][hapmap];0.91[JPT][hapmap]
rs10151464	0.91[JPT][hapmap]
rs10431718	0.88[CHD][hapmap];0.91[JPT][hapmap]
rs1045060	0.85[CHD][hapmap];0.90[JPT][hapmap]
rs10459453	0.91[JPT][hapmap]
rs10483793	0.88[ASN][1000 genomes]
rs1073607	0.91[JPT][hapmap]
rs1078194	0.82[JPT][hapmap]
rs10873200	0.91[JPT][hapmap]
rs11158655	0.88[CHD][hapmap];0.91[JPT][hapmap]
rs11158658	0.86[JPT][hapmap]
rs12323494	0.90[JPT][hapmap]
rs12323911	0.88[CHD][hapmap];0.91[JPT][hapmap]
rs12586552	0.89[JPT][hapmap]
rs12588478	0.90[JPT][hapmap]
rs12589091	0.89[JPT][hapmap]
rs12589218	0.91[JPT][hapmap]
rs12589671	0.91[JPT][hapmap]
rs12590689	0.86[ASN][1000 genomes]
rs12590956	0.82[JPT][hapmap]
rs1318914	0.91[JPT][hapmap]
rs13379142	0.90[JPT][hapmap]
rs13379368	0.91[JPT][hapmap]
rs1535491	0.88[CHD][hapmap];0.91[JPT][hapmap]
rs1536271	0.91[JPT][hapmap]
rs1536272	0.91[JPT][hapmap]
rs17104103	0.90[CHD][hapmap];0.91[JPT][hapmap]
rs17104106	0.91[JPT][hapmap]
rs17104109	0.91[JPT][hapmap]
rs17104114	0.88[CHD][hapmap];0.82[JPT][hapmap]
rs17248357	0.85[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs17248421	0.89[ASW][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];0.86[MEX][hapmap];0.82[MKK][hapmap];0.96[YRI][hapmap];0.85[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs17248526	0.88[CHD][hapmap];0.91[JPT][hapmap]
rs17248616	0.90[JPT][hapmap]
rs1885589	0.90[JPT][hapmap]
rs1918483	1.00[CHB][hapmap];0.95[CHD][hapmap];0.91[JPT][hapmap];0.82[YRI][hapmap];0.86[ASN][1000 genomes]
rs1952337	0.83[CHB][hapmap]
rs2031563	0.85[CHD][hapmap];0.86[JPT][hapmap]
rs2039055	0.88[ASN][1000 genomes]
rs2057396	0.91[JPT][hapmap]
rs2146229	0.88[CHD][hapmap];0.91[JPT][hapmap]
rs2146230	0.88[CHD][hapmap];0.91[JPT][hapmap]
rs2236333	0.91[JPT][hapmap]
rs2274335	0.91[JPT][hapmap]
rs2274338	0.91[JPT][hapmap]
rs2281676	0.97[ASN][1000 genomes]
rs2295903	0.87[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs28368552	0.81[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs28662990	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs3752993	0.95[CHB][hapmap];0.97[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap]
rs3759755	0.85[CHD][hapmap];0.91[JPT][hapmap]
rs3818467	0.85[CHD][hapmap];0.91[JPT][hapmap]
rs3866760	1.00[CHB][hapmap];0.97[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.99[ASN][1000 genomes]
rs4058254	0.86[JPT][hapmap]
rs58221168	0.80[ASN][1000 genomes]
rs6573752	1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[JPT][hapmap];0.92[ASN][1000 genomes]
rs6573754	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6573755	0.89[ASW][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];0.86[MEX][hapmap];0.82[MKK][hapmap];0.96[YRI][hapmap];0.85[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs6573760	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs7141519	0.95[CHB][hapmap];0.97[CHD][hapmap];0.91[JPT][hapmap]
rs7146638	0.88[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];0.85[MEX][hapmap];0.91[MKK][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs7147207	0.94[ASN][1000 genomes]
rs7147534	0.94[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs7148044	0.89[ASN][1000 genomes]
rs7148425	0.89[ASN][1000 genomes]
rs7149535	0.91[JPT][hapmap]
rs7150089	0.90[ASN][1000 genomes]
rs7150934	0.88[ASN][1000 genomes]
rs7151898	0.94[ASN][1000 genomes]
rs7152217	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7152231	0.91[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs7152903	0.88[CHD][hapmap];0.91[JPT][hapmap]
rs7156119	0.90[ASN][1000 genomes]
rs7156441	0.85[CHD][hapmap];0.90[JPT][hapmap]
rs7161664	0.95[CHB][hapmap];0.97[CHD][hapmap];0.91[JPT][hapmap]
rs7493580	0.88[ASN][1000 genomes]
rs768770	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs8004148	0.90[CHD][hapmap];0.81[JPT][hapmap]
rs8004488	0.88[CHD][hapmap];0.82[JPT][hapmap]
rs8005981	0.81[ASN][1000 genomes]
rs8006281	0.84[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs8006391	0.90[JPT][hapmap]
rs8006519	0.82[CHD][hapmap]
rs8008236	0.91[JPT][hapmap]
rs8008619	0.85[CHD][hapmap];0.91[JPT][hapmap]
rs8009087	0.84[ASN][1000 genomes]
rs8009318	0.91[JPT][hapmap]
rs8010261	1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[JPT][hapmap];0.92[ASN][1000 genomes]
rs8013724	0.86[ASN][1000 genomes]
rs8014966	0.91[JPT][hapmap]
rs8015862	0.91[JPT][hapmap]
rs8016037	0.88[CHD][hapmap];0.91[JPT][hapmap]
rs8019510	0.95[CHB][hapmap];0.91[JPT][hapmap]
rs8021896	0.88[CHD][hapmap];0.91[JPT][hapmap]
rs9323494	0.86[ASN][1000 genomes]
rs9743911	0.91[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:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7154905	EIF2S1	cis	multi-tissue	Pritchard
rs7154905	EIF2S1	cis	lymphoblastoid	seeQTL

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:67591400-67640000	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr14:67600800-67647400	Weak transcription	Fetal Kidney	kidney
3	chr14:67613000-67640200	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr14:67614400-67653200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr14:67618400-67658200	Weak transcription	Brain Angular Gyrus	brain
6	chr14:67630000-67645600	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr14:67631600-67645800	Weak transcription	Psoas Muscle	Psoas
8	chr14:67632400-67640000	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr14:67633200-67640000	Weak transcription	Brain Anterior Caudate	brain
10	chr14:67633200-67640000	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr14:67633200-67645400	Weak transcription	Rectal Smooth Muscle	rectum
12	chr14:67633600-67640000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr14:67633600-67640200	Weak transcription	Colon Smooth Muscle	Colon
14	chr14:67634600-67653200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr14:67635000-67640000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr14:67635000-67652800	Weak transcription	NHEK	skin
17	chr14:67635000-67653200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr14:67635200-67645200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr14:67635800-67640000	Weak transcription	Fetal Lung	lung
20	chr14:67636200-67645400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr14:67637200-67640000	Strong transcription	Brain Cingulate Gyrus	brain
22	chr14:67637600-67640000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
23	chr14:67638000-67645400	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr14:67638600-67640000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr14:67638600-67640200	ZNF genes & repeats	Fetal Intestine Small	intestine
26	chr14:67638600-67640400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr14:67639000-67640000	Weak transcription	Liver	Liver
28	chr14:67639000-67640000	Weak transcription	Ovary	ovary
29	chr14:67639000-67640200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr14:67639200-67640000	Strong transcription	Brain Hippocampus Middle	brain
31	chr14:67639200-67640000	Weak transcription	Brain Substantia Nigra	brain
32	chr14:67639200-67640000	ZNF genes & repeats	Lung	lung
33	chr14:67639200-67640200	ZNF genes & repeats	Fetal Stomach	stomach
34	chr14:67639200-67640400	ZNF genes & repeats	Duodenum Mucosa	Duodenum
35	chr14:67639400-67640000	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
36	chr14:67639400-67640000	ZNF genes & repeats	Fetal Muscle Leg	muscle
37	chr14:67639400-67640000	ZNF genes & repeats	Pancreas	Pancrea
38	chr14:67639400-67640200	ZNF genes & repeats	Fetal Brain Female	brain
39	chr14:67639400-67640400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr14:67639400-67640400	ZNF genes & repeats	Aorta	Aorta
41	chr14:67639400-67640600	ZNF genes & repeats	Brain Germinal Matrix	brain
42	chr14:67639400-67646200	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr14:67639600-67640000	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
44	chr14:67639600-67640200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr14:67639600-67640200	ZNF genes & repeats	Fetal Brain Male	brain
46	chr14:67639600-67640200	ZNF genes & repeats	Fetal Muscle Trunk	muscle
47	chr14:67639600-67640400	ZNF genes & repeats	Left Ventricle	heart
48	chr14:67639600-67647400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr14:67639600-67647400	Weak transcription	Right Ventricle	heart
50	chr14:67639600-67658600	Weak transcription	Stomach Smooth Muscle	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links