Variant report

Variant	rs4529019
Chromosome Location	chr4:47861957-47861958
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 121 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:109)

rs_ID	r²[population]
rs10020447	0.81[CEU][hapmap]
rs10025104	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10030927	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10049713	0.81[JPT][hapmap]
rs1036681	0.82[CEU][hapmap]
rs1062858	0.80[JPT][hapmap]
rs10938503	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10938506	0.81[JPT][hapmap]
rs12503789	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12504018	0.81[JPT][hapmap]
rs12506632	0.81[JPT][hapmap]
rs12507439	0.85[JPT][hapmap]
rs12651301	0.81[JPT][hapmap]
rs1371730	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1440227	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1440228	0.81[JPT][hapmap]
rs1507920	0.88[CHB][hapmap]
rs1507922	0.90[CEU][hapmap];0.94[CHB][hapmap];0.82[JPT][hapmap];0.86[EUR][1000 genomes]
rs1550444	0.81[CEU][hapmap]
rs1583808	0.94[CHB][hapmap];0.89[JPT][hapmap];0.90[ASN][1000 genomes]
rs16860723	1.00[CHB][hapmap];0.89[JPT][hapmap];0.87[ASN][1000 genomes]
rs16860815	0.89[CHB][hapmap]
rs1812964	0.86[CEU][hapmap]
rs1822030	0.80[JPT][hapmap]
rs1866689	0.80[JPT][hapmap]
rs1972883	0.81[CEU][hapmap]
rs2014934	0.82[CEU][hapmap]
rs2033893	0.81[JPT][hapmap]
rs2033895	0.81[CEU][hapmap]
rs2033897	1.00[CHB][hapmap];0.89[JPT][hapmap];0.90[ASN][1000 genomes]
rs2033898	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2053404	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2119207	0.82[CEU][hapmap]
rs2289433	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2352145	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2352463	0.82[CEU][hapmap]
rs2352466	0.82[CEU][hapmap]
rs321620	0.91[CEU][hapmap];0.94[CHB][hapmap]
rs3762858	0.81[CEU][hapmap]
rs3762859	0.81[CEU][hapmap]
rs3811761	0.82[CEU][hapmap]
rs3845160	0.82[CEU][hapmap]
rs4308343	0.82[CEU][hapmap]
rs4365692	0.81[CEU][hapmap]
rs4565052	0.81[JPT][hapmap]
rs4694867	0.94[CHB][hapmap];0.89[JPT][hapmap];0.90[ASN][1000 genomes]
rs4694868	0.81[CEU][hapmap]
rs4694871	0.81[CEU][hapmap]
rs4694872	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];0.96[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4695277	0.90[ASN][1000 genomes]
rs4695285	0.94[CHB][hapmap];0.89[JPT][hapmap];0.90[ASN][1000 genomes]
rs4695286	0.94[CHB][hapmap];0.89[JPT][hapmap];0.90[ASN][1000 genomes]
rs4695287	0.81[CEU][hapmap]
rs4695290	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4695292	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4695296	0.82[CEU][hapmap]
rs4695300	0.94[CHB][hapmap];0.89[JPT][hapmap];0.87[ASN][1000 genomes]
rs4695302	0.82[CEU][hapmap]
rs4695303	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4695306	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4695307	0.89[CHB][hapmap];0.89[JPT][hapmap];0.86[ASN][1000 genomes]
rs4695308	0.86[ASN][1000 genomes]
rs4695309	0.81[CEU][hapmap]
rs4695312	0.82[CEU][hapmap]
rs57010305	0.87[ASN][1000 genomes]
rs58511183	0.87[ASN][1000 genomes]
rs60427744	0.87[ASN][1000 genomes]
rs60515154	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6414687	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6447586	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6447592	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6447593	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6447599	0.85[CEU][hapmap]
rs6811385	0.94[CHB][hapmap];0.89[JPT][hapmap];0.87[ASN][1000 genomes]
rs6815975	0.82[CEU][hapmap]
rs6816082	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6818556	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6822668	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6823184	0.81[JPT][hapmap]
rs6823698	0.80[JPT][hapmap]
rs6826190	0.82[CEU][hapmap]
rs6827508	1.00[CEU][hapmap];0.87[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6829073	0.81[CEU][hapmap]
rs6832334	0.81[CEU][hapmap]
rs6833320	0.81[CEU][hapmap]
rs6844286	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6850142	0.81[CEU][hapmap]
rs707723	0.82[CEU][hapmap]
rs73238638	0.89[ASN][1000 genomes]
rs73238639	0.90[ASN][1000 genomes]
rs73244433	0.87[ASN][1000 genomes]
rs73244436	0.89[ASN][1000 genomes]
rs73244437	0.86[ASN][1000 genomes]
rs73244438	0.87[ASN][1000 genomes]
rs73244439	0.87[ASN][1000 genomes]
rs73244442	0.84[ASN][1000 genomes]
rs7663935	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7668778	0.82[CEU][hapmap]
rs7670219	0.80[CEU][hapmap]
rs7672090	0.86[CEU][hapmap]
rs7687363	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7690562	1.00[CEU][hapmap];0.87[CHB][hapmap];0.94[JPT][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8180146	0.80[JPT][hapmap]
rs893863	0.82[CEU][hapmap]
rs893864	0.81[CEU][hapmap]
rs920462	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs920463	0.82[CEU][hapmap]
rs9291317	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9683791	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008515	chr4:47488431-47906835	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Active TSS Flanking 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 miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv948568	chr4:47488431-47907524	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv1004939	chr4:47488573-47901460	Bivalent Enhancer Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv537080	chr4:47488573-47901460	Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv997471	chr4:47489412-47895223	Weak transcription Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
6	nsv998892	chr4:47493552-47863354	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
7	nsv537081	chr4:47493552-47863354	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
8	nsv1000337	chr4:47493907-47902019	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking 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 miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
9	nsv594118	chr4:47560386-47917730	Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
10	nsv829924	chr4:47670905-47866665	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv4328	chr4:47816467-47862253	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	esv3447039	chr4:47822266-48285222	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS 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	34 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs4529019	CNGA1	cis	Heart Left Ventricle	GTEx
rs4529019	CNGA1	cis	Muscle Skeletal	GTEx
rs4529019	CNGA1	cis	Thyroid	GTEx

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:47839800-47874800	Weak transcription	A549	lung
2	chr4:47839800-47875000	Weak transcription	Brain Angular Gyrus	brain
3	chr4:47839800-47885800	Weak transcription	Lung	lung
4	chr4:47840000-47874600	Weak transcription	Brain Substantia Nigra	brain
5	chr4:47840000-47874800	Weak transcription	Brain Cingulate Gyrus	brain
6	chr4:47840000-47875400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr4:47840000-47875600	Weak transcription	Rectal Smooth Muscle	rectum
8	chr4:47840000-47886800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr4:47840200-47866600	Weak transcription	Esophagus	oesophagus
10	chr4:47840200-47867000	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr4:47840200-47869600	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr4:47840200-47874600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr4:47840200-47874800	Weak transcription	Psoas Muscle	Psoas
14	chr4:47840200-47881600	Weak transcription	Stomach Mucosa	stomach
15	chr4:47840200-47885200	Weak transcription	Aorta	Aorta
16	chr4:47840200-47885800	Weak transcription	Pancreas	Pancrea
17	chr4:47840400-47866600	Weak transcription	Stomach Smooth Muscle	stomach
18	chr4:47840400-47874600	Weak transcription	Brain Hippocampus Middle	brain
19	chr4:47840400-47874600	Weak transcription	Fetal Brain Male	brain
20	chr4:47840400-47875400	Weak transcription	Small Intestine	intestine
21	chr4:47840400-47875600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr4:47840600-47874800	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr4:47840600-47875200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr4:47840800-47867600	Weak transcription	Fetal Intestine Small	intestine
25	chr4:47840800-47874600	Weak transcription	Brain Germinal Matrix	brain
26	chr4:47840800-47874800	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr4:47840800-47875400	Weak transcription	Right Ventricle	heart
28	chr4:47841200-47874800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr4:47841200-47874800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr4:47841400-47874600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr4:47841400-47875600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr4:47841600-47874600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr4:47841800-47874600	Weak transcription	Fetal Heart	heart
34	chr4:47841800-47874600	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr4:47841800-47880000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
36	chr4:47843400-47874600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr4:47843800-47897000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
38	chr4:47845800-47873400	Weak transcription	Fetal Brain Female	brain
39	chr4:47846400-47875200	Weak transcription	Fetal Muscle Leg	muscle
40	chr4:47846600-47869800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr4:47846800-47874400	Weak transcription	Fetal Muscle Trunk	muscle
42	chr4:47846800-47874600	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr4:47846800-47876000	Weak transcription	NHEK	skin
44	chr4:47847000-47868400	Weak transcription	Fetal Stomach	stomach
45	chr4:47850000-47874800	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr4:47850400-47866600	Weak transcription	Primary T cells fromperipheralblood	blood
47	chr4:47851800-47875200	Weak transcription	Colon Smooth Muscle	Colon
48	chr4:47852800-47875000	Weak transcription	Fetal Thymus	thymus
49	chr4:47853000-47874400	Weak transcription	Rectal Mucosa Donor 29	rectum
50	chr4:47853200-47866800	Weak transcription	Placenta	Placenta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links