Variant report

Variant	rs9873891
Chromosome Location	chr3:145948043-145948044
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 98 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:93)

rs_ID	r²[population]
rs10222588	0.87[ASN][1000 genomes]
rs10737947	1.00[CHB][hapmap];0.96[YRI][hapmap];0.97[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs10804709	0.86[ASN][1000 genomes]
rs10804710	0.95[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs10935611	0.94[CHB][hapmap];0.86[ASN][1000 genomes]
rs10935613	0.97[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs10935614	0.95[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs10935615	0.91[ASN][1000 genomes]
rs10935616	0.94[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs11709096	0.95[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs11716310	0.84[ASN][1000 genomes]
rs11915448	1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs11919011	0.95[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs11926517	0.87[ASN][1000 genomes]
rs12487353	0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12632757	0.84[ASN][1000 genomes]
rs12633074	0.94[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs1398125	0.81[AFR][1000 genomes]
rs1398529	0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1512078	0.95[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs1512079	0.91[ASN][1000 genomes]
rs1512080	1.00[ASN][1000 genomes]
rs1512081	1.00[CHB][hapmap];0.92[YRI][hapmap];0.94[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs1512888	0.84[ASN][1000 genomes]
rs1512890	1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs1512893	0.83[ASN][1000 genomes]
rs1606434	1.00[ASN][1000 genomes]
rs1877511	1.00[CHB][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs1913184	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs2036980	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs2175544	1.00[CHB][hapmap];0.90[ASN][1000 genomes]
rs2175545	0.93[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs2867081	0.95[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs2867082	1.00[ASN][1000 genomes]
rs2867083	0.95[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs2867084	0.89[ASN][1000 genomes]
rs2903478	0.84[ASN][1000 genomes]
rs2903479	1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs3762686	0.93[CHB][hapmap];0.84[ASN][1000 genomes]
rs3762688	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs3792338	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs3804648	0.84[ASN][1000 genomes]
rs3804654	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs3914252	0.84[ASN][1000 genomes]
rs4273339	1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs4475004	1.00[CHB][hapmap];0.93[JPT][hapmap];0.98[ASN][1000 genomes]
rs4488802	1.00[CHB][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs4610193	0.87[ASN][1000 genomes]
rs4681306	0.91[ASN][1000 genomes]
rs4681307	0.90[ASN][1000 genomes]
rs4681308	0.92[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs4681310	0.87[ASN][1000 genomes]
rs6440421	1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6440422	0.91[ASN][1000 genomes]
rs6770057	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6770163	1.00[CHB][hapmap];0.85[YRI][hapmap];0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6770278	1.00[CHB][hapmap];0.89[YRI][hapmap];0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6775520	0.85[AFR][1000 genomes]
rs6792732	0.94[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs6805377	0.93[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs7430290	0.93[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs7612683	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs7621841	1.00[CHB][hapmap];0.92[YRI][hapmap];0.92[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs7632412	0.94[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs7633252	0.81[ASN][1000 genomes]
rs7634568	0.94[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs7643778	1.00[CHB][hapmap];0.92[YRI][hapmap];0.92[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs925464	0.84[ASN][1000 genomes]
rs9756128	0.84[ASN][1000 genomes]
rs9809892	0.84[ASN][1000 genomes]
rs9813122	0.92[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs9822280	0.84[ASN][1000 genomes]
rs9825776	0.95[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs9826132	0.92[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs9826360	0.95[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs9826591	1.00[ASN][1000 genomes]
rs9830892	1.00[ASN][1000 genomes]
rs9836419	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9838801	0.86[ASN][1000 genomes]
rs9838866	1.00[CHB][hapmap];0.90[ASN][1000 genomes]
rs9839724	0.84[ASN][1000 genomes]
rs9839874	0.94[CHB][hapmap];0.84[ASN][1000 genomes]
rs9845890	0.86[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs9850566	0.84[ASN][1000 genomes]
rs9851511	0.92[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs9855695	1.00[CHB][hapmap];0.92[YRI][hapmap];0.90[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs9858823	0.98[ASN][1000 genomes]
rs9859273	1.00[CHB][hapmap];0.93[JPT][hapmap];0.98[ASN][1000 genomes]
rs9863647	1.00[CHB][hapmap];0.92[YRI][hapmap];0.94[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs9867851	0.91[ASN][1000 genomes]
rs9875799	0.92[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs9877004	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs9881755	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877614	chr3:145903426-146025896	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
2	nsv877615	chr3:145910430-145988231	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
3	nsv877616	chr3:145921954-145983688	Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	esv3333601	chr3:145940702-146068210	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	esv3416330	chr3:145941029-146068457	Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:145925400-145952800	Weak transcription	Primary hematopoietic stem cells	blood
2	chr3:145925600-145950800	Weak transcription	Fetal Kidney	kidney
3	chr3:145934600-145952200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr3:145940600-145953000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr3:145940600-145953600	Weak transcription	NHDF-Ad	bronchial
6	chr3:145941400-145948400	Weak transcription	Osteobl	bone
7	chr3:145941600-145952200	Weak transcription	Left Ventricle	heart
8	chr3:145941600-145952600	Weak transcription	Fetal Intestine Small	intestine
9	chr3:145941600-145954000	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr3:145942200-145953400	Weak transcription	HUVEC	blood vessel
11	chr3:145945200-145959800	Weak transcription	Ovary	ovary
12	chr3:145945400-145948200	Weak transcription	Aorta	Aorta
13	chr3:145946000-145952400	Weak transcription	Fetal Stomach	stomach
14	chr3:145946200-145952600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr3:145946400-145953000	Weak transcription	Stomach Smooth Muscle	stomach
16	chr3:145947200-145953000	Weak transcription	Adipose Nuclei	Adipose
17	chr3:145947400-145950200	Weak transcription	Liver	Liver
18	chr3:145947400-145953200	Weak transcription	Fetal Intestine Large	intestine
19	chr3:145947800-145949400	Strong transcription	Fetal Lung	lung
20	chr3:145948000-145967800	Weak transcription	Placenta Amnion	Placenta Amnion

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