Variant report

Variant	rs10732343
Chromosome Location	chr9:2390378-2390379
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 95 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs10118478	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10738682	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10738683	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10757450	0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10757451	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10757457	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10757459	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10811972	0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10811975	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10811994	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10811995	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10811996	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10811997	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10811999	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10812000	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10966115	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10966132	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10966137	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10966139	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10966144	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11791024	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11795121	0.80[AMR][1000 genomes]
rs12000541	0.86[ASN][1000 genomes]
rs1331830	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1331832	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1331833	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1331834	0.96[ASN][1000 genomes]
rs1331835	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1331836	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1412184	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1412185	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1412186	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1412188	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1576719	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1576720	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1831548	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2104858	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2150835	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2150836	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2183811	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2183812	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2183814	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2210399	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2376125	0.97[ASN][1000 genomes]
rs4363251	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4363252	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4740677	0.83[AMR][1000 genomes]
rs4740680	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4741692	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4741694	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4741695	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4741699	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4741700	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4741701	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4741703	0.92[ASN][1000 genomes]
rs4741704	0.88[ASN][1000 genomes]
rs6475762	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6475766	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7019582	0.87[ASN][1000 genomes]
rs7021052	0.80[AMR][1000 genomes]
rs7023637	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7025116	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7028293	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7038869	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7041232	0.87[ASN][1000 genomes]
rs7470470	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7847686	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7849851	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7858528	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7858645	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs866991	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs872039	0.82[EUR][1000 genomes]
rs959378	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs959379	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs959380	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs959381	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1020530	chr9:1870197-2658587	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv530929	chr9:1998911-2925112	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv466078	chr9:2218129-2621030	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv613126	chr9:2218129-2621030	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv613128	chr9:2253678-2419538	Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1016677	chr9:2253741-2415423	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1016401	chr9:2255397-2410590	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv529508	chr9:2267812-2684272	Bivalent/Poised TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
9	nsv892063	chr9:2291635-2419538	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv892064	chr9:2301610-2447910	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	nsv466080	chr9:2318486-2432800	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv613131	chr9:2318486-2432800	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	nsv1015425	chr9:2324332-2408041	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	nsv539932	chr9:2324332-2408041	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
15	nsv531563	chr9:2324333-2501030	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
16	nsv1021309	chr9:2336185-2506959	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
17	nsv892065	chr9:2342366-2424322	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
18	nsv466081	chr9:2353522-2596783	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
19	nsv613132	chr9:2353522-2596783	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs10732343	RP11-125B21.2	cis	Artery Tibial	GTEx
rs10732343	VLDLR	cis	Artery Tibial	GTEx

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:2387200-2394600	Weak transcription	Adipose Nuclei	Adipose
2	chr9:2389000-2390400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr9:2389800-2390400	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr9:2390000-2390400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr9:2390200-2390400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr9:2390200-2390400	Enhancers	Ovary	ovary

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