Variant report

Variant	rs2382532
Chromosome Location	chr9:15687846-15687847
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 150 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:136)

rs_ID	r²[population]
rs10118359	0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10121393	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10121591	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10122339	0.97[ASN][1000 genomes]
rs10123042	0.88[ASN][1000 genomes]
rs1039813	0.82[EUR][1000 genomes]
rs1039814	0.82[EUR][1000 genomes]
rs10481557	0.84[EUR][1000 genomes]
rs10733295	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10738402	0.86[EUR][1000 genomes]
rs10738403	0.85[EUR][1000 genomes]
rs10738404	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10738405	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10738406	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10756674	0.81[EUR][1000 genomes]
rs10756676	0.83[EUR][1000 genomes]
rs10756677	0.84[EUR][1000 genomes]
rs10756678	0.84[EUR][1000 genomes]
rs10756679	0.85[EUR][1000 genomes]
rs10756680	0.86[EUR][1000 genomes]
rs10756686	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10756687	0.84[AFR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10756688	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10756689	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10756690	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10756692	0.87[EUR][1000 genomes]
rs10756693	0.87[EUR][1000 genomes]
rs10756694	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10756695	0.89[EUR][1000 genomes]
rs10756696	0.88[EUR][1000 genomes]
rs10756697	0.87[EUR][1000 genomes]
rs10810399	0.81[EUR][1000 genomes]
rs10810400	0.81[EUR][1000 genomes]
rs10810401	0.84[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs10810402	0.81[EUR][1000 genomes]
rs10810405	0.81[EUR][1000 genomes]
rs10810408	0.83[EUR][1000 genomes]
rs10810409	0.87[EUR][1000 genomes]
rs10810416	0.82[ASN][1000 genomes]
rs10810419	0.82[ASN][1000 genomes]
rs10810422	0.88[ASN][1000 genomes]
rs10810424	0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10810426	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10810427	0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10810428	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10810431	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10810432	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10810433	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10810434	0.90[EUR][1000 genomes]
rs10810435	0.88[EUR][1000 genomes]
rs10810436	0.88[EUR][1000 genomes]
rs10962066	0.82[EUR][1000 genomes]
rs10962070	0.81[EUR][1000 genomes]
rs10962098	0.84[EUR][1000 genomes]
rs10962099	0.84[EUR][1000 genomes]
rs10962106	0.82[ASN][1000 genomes]
rs10962110	0.89[EUR][1000 genomes]
rs10962124	0.88[EUR][1000 genomes]
rs11789538	0.85[EUR][1000 genomes]
rs11789563	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11791627	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11792937	0.82[ASN][1000 genomes]
rs12340969	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13291638	0.87[EUR][1000 genomes]
rs13301516	0.82[ASN][1000 genomes]
rs1355171	0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1396707	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1396708	0.89[EUR][1000 genomes]
rs1509310	0.89[EUR][1000 genomes]
rs1533040	0.81[AFR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1553728	0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1812686	0.84[EUR][1000 genomes]
rs1848582	0.82[ASN][1000 genomes]
rs2055772	0.83[EUR][1000 genomes]
rs2136355	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2175082	0.86[AFR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2382534	0.90[EUR][1000 genomes]
rs2382538	0.85[EUR][1000 genomes]
rs28403566	0.90[ASN][1000 genomes]
rs35146544	0.85[EUR][1000 genomes]
rs3955162	0.81[EUR][1000 genomes]
rs4339736	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4448380	0.83[EUR][1000 genomes]
rs4740615	0.83[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs4740618	0.83[EUR][1000 genomes]
rs4740619	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4740620	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4740621	0.85[AFR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4740622	0.87[EUR][1000 genomes]
rs4741515	0.82[EUR][1000 genomes]
rs4741517	0.83[EUR][1000 genomes]
rs4741519	0.88[EUR][1000 genomes]
rs4741520	0.83[EUR][1000 genomes]
rs4741528	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4741529	0.89[EUR][1000 genomes]
rs4741534	0.90[EUR][1000 genomes]
rs4741535	0.86[EUR][1000 genomes]
rs6474942	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6474944	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6474945	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6474946	0.80[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6474953	0.90[EUR][1000 genomes]
rs6474954	0.90[EUR][1000 genomes]
rs6474955	0.90[EUR][1000 genomes]
rs7019430	0.85[EUR][1000 genomes]
rs7023275	0.84[ASN][1000 genomes]
rs7024640	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7025669	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7030846	0.89[ASN][1000 genomes]
rs7031365	0.82[ASN][1000 genomes]
rs7032755	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7032877	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7033236	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7034484	0.89[ASN][1000 genomes]
rs7035863	0.96[ASN][1000 genomes]
rs7036172	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7036674	0.85[AFR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7036875	0.88[ASN][1000 genomes]
rs7042475	0.82[ASN][1000 genomes]
rs7044122	0.83[EUR][1000 genomes]
rs7046351	0.88[ASN][1000 genomes]
rs7049101	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7049176	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7389047	0.85[EUR][1000 genomes]
rs7847144	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7848511	0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7851056	0.82[ASN][1000 genomes]
rs7854714	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7855235	0.90[EUR][1000 genomes]
rs7859780	0.86[EUR][1000 genomes]
rs7860623	0.81[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs7861004	0.89[EUR][1000 genomes]
rs7863088	0.86[EUR][1000 genomes]
rs7868779	0.84[EUR][1000 genomes]
rs7874533	0.83[EUR][1000 genomes]
rs9696751	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv892625	chr9:15326251-16064850	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv892626	chr9:15389610-15694690	Flanking Active TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv892627	chr9:15397969-15909450	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
4	nsv892630	chr9:15554960-15694690	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	esv2752286	chr9:15578017-15794897	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv892631	chr9:15590116-15694690	Weak transcription ZNF genes & repeats Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
7	nsv892632	chr9:15590116-15869845	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv892633	chr9:15604746-15889411	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv613656	chr9:15615321-15696501	Enhancers Strong transcription ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv466262	chr9:15615321-15727518	ZNF genes & repeats Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	nsv613657	chr9:15615321-15727518	ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	nsv613658	chr9:15636260-15727518	Strong transcription Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	nsv466263	chr9:15641279-15726057	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
14	nsv613659	chr9:15641279-15726057	Strong transcription ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15645600-15689200	Weak transcription	Primary hematopoietic stem cells	blood
2	chr9:15655200-15691600	Weak transcription	Thymus	Thymus
3	chr9:15669000-15720800	Weak transcription	Gastric	stomach
4	chr9:15672000-15688600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr9:15675000-15699000	Weak transcription	Left Ventricle	heart
6	chr9:15676400-15688600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr9:15676600-15725000	Weak transcription	Pancreas	Pancrea
8	chr9:15677000-15695200	Weak transcription	Fetal Thymus	thymus
9	chr9:15679800-15746800	Weak transcription	Ovary	ovary
10	chr9:15684000-15697000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr9:15687600-15746600	Weak transcription	Aorta	Aorta

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