Variant report

Variant	rs35463506
Chromosome Location	chr5:119484510-119484511
allele	-/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 132 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:117)

rs_ID	r²[population]
rs10043143	0.83[EUR][1000 genomes]
rs10052192	0.83[EUR][1000 genomes]
rs10052564	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10053118	0.92[ASN][1000 genomes]
rs10066059	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10079429	0.92[ASN][1000 genomes]
rs1031130	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1031131	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10900735	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1191736	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11951475	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11951498	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12517429	0.92[ASN][1000 genomes]
rs12520161	0.92[ASN][1000 genomes]
rs12520785	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12520817	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12521813	0.92[ASN][1000 genomes]
rs12522508	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12522857	0.82[EUR][1000 genomes]
rs12523293	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13183113	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1348474	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1348478	0.82[ASN][1000 genomes]
rs1348479	0.82[ASN][1000 genomes]
rs1373317	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1373318	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1373320	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1373324	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1443966	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1443969	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1443970	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1443980	0.82[ASN][1000 genomes]
rs1443981	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1443985	0.82[ASN][1000 genomes]
rs1443986	0.82[ASN][1000 genomes]
rs1443987	0.82[ASN][1000 genomes]
rs1470349	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17146058	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17146063	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17146068	0.83[ASN][1000 genomes]
rs17146098	0.81[ASN][1000 genomes]
rs17146149	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17146179	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17146184	0.92[ASN][1000 genomes]
rs1862306	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1862307	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1907193	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1907194	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1974787	0.83[EUR][1000 genomes]
rs1981819	0.92[ASN][1000 genomes]
rs2053622	0.83[ASN][1000 genomes]
rs2059093	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2130738	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2130739	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2161303	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2166013	0.82[ASN][1000 genomes]
rs255792	0.84[EUR][1000 genomes]
rs255803	0.84[EUR][1000 genomes]
rs28635608	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2897117	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs35236191	0.80[ASN][1000 genomes]
rs35648087	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs35758661	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3991623	0.80[EUR][1000 genomes]
rs41447148	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4446498	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4446499	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4868423	0.92[ASN][1000 genomes]
rs55635066	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56151766	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56186068	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56352443	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs57510292	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs58036644	0.84[EUR][1000 genomes]
rs59845464	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs60408531	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs60547170	0.84[ASN][1000 genomes]
rs60772350	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61395607	0.87[ASN][1000 genomes]
rs62376993	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs62376998	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62377003	0.81[ASN][1000 genomes]
rs62377004	0.84[EUR][1000 genomes]
rs62377005	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6595211	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6866827	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6868570	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6868780	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6873570	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6874351	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6874504	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6877170	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6879182	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6882395	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6883507	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6888177	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6888446	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6889996	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6895104	0.85[EUR][1000 genomes]
rs6898633	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs718734	0.83[EUR][1000 genomes]
rs718735	0.83[EUR][1000 genomes]
rs719191	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73266681	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7702005	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7705480	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7707700	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7722633	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7730558	0.92[ASN][1000 genomes]
rs9327125	0.83[ASN][1000 genomes]
rs9327129	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs953189	0.81[ASN][1000 genomes]
rs982358	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs982605	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs982606	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs982607	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs994630	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024455	chr5:118770429-119487982	Strong transcription Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1016271	chr5:118836891-119487982	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1023146	chr5:119301891-119623417	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv537883	chr5:119301891-119623417	Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	esv3331559	chr5:119306944-119536554	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv532200	chr5:119317901-120102513	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv882780	chr5:119332670-119488924	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	nsv882781	chr5:119369334-119557828	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv599600	chr5:119399177-119507243	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	nsv1026457	chr5:119406305-119493661	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	nsv537885	chr5:119406305-119493661	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
12	nsv432803	chr5:119419101-119659101	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	esv2762547	chr5:119427979-119487383	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv1016024	chr5:119460796-119509057	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
15	nsv1018247	chr5:119469805-119511846	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:119482400-119487600	Weak transcription	NHLF	lung
2	chr5:119483000-119486600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr5:119483000-119486600	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr5:119483000-119487000	Weak transcription	Osteobl	bone
5	chr5:119483000-119487400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr5:119483000-119487400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr5:119483000-119487600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr5:119483200-119486600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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