Variant report

Variant	rs4968250
Chromosome Location	chr17:45045351-45045352
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 90 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:79)

rs_ID	r²[population]
rs1047779	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1052504	0.98[ASN][1000 genomes]
rs1052586	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10853085	0.98[ASN][1000 genomes]
rs10853087	0.98[ASN][1000 genomes]
rs11079742	0.87[EUR][1000 genomes]
rs11079745	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11652318	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11654971	0.98[ASN][1000 genomes]
rs11656362	0.99[ASN][1000 genomes]
rs11658276	0.96[ASN][1000 genomes]
rs11869840	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12601886	0.98[ASN][1000 genomes]
rs12940071	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1618989	0.97[ASN][1000 genomes]
rs1623402	0.98[ASN][1000 genomes]
rs1662576	0.98[ASN][1000 genomes]
rs1662577	0.98[ASN][1000 genomes]
rs1662594	0.98[ASN][1000 genomes]
rs1662596	0.98[ASN][1000 genomes]
rs1662597	0.96[ASN][1000 genomes]
rs17608961	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1867237	0.98[ASN][1000 genomes]
rs197912	0.85[ASN][1000 genomes]
rs197913	0.87[ASN][1000 genomes]
rs197915	0.90[ASN][1000 genomes]
rs197917	0.96[ASN][1000 genomes]
rs197918	0.98[ASN][1000 genomes]
rs197919	0.98[ASN][1000 genomes]
rs197925	0.96[ASN][1000 genomes]
rs197926	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2003538	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2003539	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2191033	0.98[ASN][1000 genomes]
rs2316330	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2317997	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28553405	0.87[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2920396	0.98[ASN][1000 genomes]
rs2920397	0.98[ASN][1000 genomes]
rs35707546	0.96[ASN][1000 genomes]
rs3760377	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3785888	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3809854	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3851784	0.98[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3851785	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3851786	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3851787	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4381655	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4602097	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4968248	0.95[ASN][1000 genomes]
rs4968285	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4968286	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4968287	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4968288	0.98[ASN][1000 genomes]
rs4968290	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61671555	0.84[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs62075889	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62075896	0.83[EUR][1000 genomes]
rs6504622	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7213526	0.96[ASN][1000 genomes]
rs7216991	0.84[EUR][1000 genomes]
rs7225428	0.98[ASN][1000 genomes]
rs7342957	0.98[ASN][1000 genomes]
rs736603	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs736604	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs740617	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs758391	0.84[EUR][1000 genomes]
rs758392	0.83[EUR][1000 genomes]
rs9303532	0.84[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs9889741	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9889762	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9893713	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9898527	0.84[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs9898981	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9901977	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9910899	0.81[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs9911366	0.84[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs9911967	0.98[ASN][1000 genomes]
rs9912794	0.84[AFR][1000 genomes];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3492820	chr17:44174959-45161556	Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	esv3492821	chr17:44174959-45161556	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
3	esv3502492	chr17:44305975-45169159	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	esv3502493	chr17:44305975-45169159	Active TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
5	nsv531823	chr17:44485771-45067769	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
6	nsv908562	chr17:44828931-45102413	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
7	nsv949295	chr17:44836653-45080757	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	24 gene(s)	inside rSNPs	diseases
8	nsv1067211	chr17:44979111-45057620	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
9	nsv543378	chr17:44979111-45057620	Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
10	nsv833466	chr17:45020360-45204537	Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
11	nsv1062983	chr17:45030095-45789543	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers 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	70 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4968250	GOSR2	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45021800-45051800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr17:45023000-45045400	Weak transcription	Ovary	ovary
3	chr17:45027400-45054000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr17:45028600-45048800	Weak transcription	Esophagus	oesophagus
5	chr17:45034600-45045600	Weak transcription	Fetal Intestine Small	intestine
6	chr17:45036400-45045800	Weak transcription	Fetal Brain Female	brain
7	chr17:45036400-45052400	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr17:45036600-45054400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr17:45037400-45055800	Weak transcription	Aorta	Aorta
10	chr17:45037800-45052200	Weak transcription	Brain Cingulate Gyrus	brain
11	chr17:45038000-45052600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr17:45040200-45045800	Weak transcription	Spleen	Spleen
13	chr17:45040200-45047800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr17:45040200-45055600	Weak transcription	Pancreas	Pancrea
15	chr17:45042800-45051200	Weak transcription	Fetal Muscle Leg	muscle
16	chr17:45042800-45052800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr17:45043000-45049600	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr17:45043000-45054000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr17:45043600-45046600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
20	chr17:45043800-45046400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr17:45044000-45045400	Weak transcription	Fetal Stomach	stomach
22	chr17:45044000-45049600	Weak transcription	Stomach Smooth Muscle	stomach
23	chr17:45044200-45046200	Weak transcription	Primary B cells from peripheral blood	blood
24	chr17:45044400-45047000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr17:45044600-45045400	Strong transcription	Skeletal Muscle Male	skeletal muscle
26	chr17:45044600-45049600	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr17:45045000-45047000	Strong transcription	Primary T helper cells fromperipheralblood	blood
28	chr17:45045200-45046200	Strong transcription	Adipose Nuclei	Adipose
29	chr17:45045200-45046200	Strong transcription	HepG2	liver

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