Variant report

Variant	rs3739569
Chromosome Location	chr9:18574694-18574695
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10733355	0.82[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs10756968	0.90[CEU][hapmap];0.82[CHB][hapmap];0.86[JPT][hapmap];0.80[ASN][1000 genomes]
rs10756969	0.96[CHB][hapmap];0.91[JPT][hapmap];0.92[YRI][hapmap];0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10756970	0.96[CHB][hapmap];0.91[JPT][hapmap];0.92[YRI][hapmap];0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10756973	0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs10756974	0.91[CHB][hapmap];0.87[ASN][1000 genomes]
rs10756975	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10756976	1.00[CEU][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10756977	0.87[CEU][hapmap];0.83[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs10810982	0.90[CEU][hapmap];0.82[JPT][hapmap]
rs10810984	0.82[JPT][hapmap]
rs10810985	0.84[JPT][hapmap]
rs10810986	0.83[CHB][hapmap];0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs10810987	0.83[CHB][hapmap];0.87[JPT][hapmap];0.84[YRI][hapmap];0.80[ASN][1000 genomes]
rs10810988	1.00[CHB][hapmap];0.82[JPT][hapmap];0.83[YRI][hapmap];0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10810989	0.91[CHB][hapmap];0.80[JPT][hapmap];0.87[YRI][hapmap];0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10963633	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs10963634	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10963635	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10963639	0.91[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs12345096	0.83[CHB][hapmap];0.87[JPT][hapmap];0.84[YRI][hapmap];0.81[ASN][1000 genomes]
rs12345939	0.95[CHB][hapmap];0.86[JPT][hapmap];0.90[YRI][hapmap];0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12553147	0.82[JPT][hapmap]
rs12685259	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs13290343	0.90[CEU][hapmap]
rs13292240	0.95[CHB][hapmap];0.84[YRI][hapmap];0.83[AFR][1000 genomes]
rs1341066	0.82[JPT][hapmap]
rs1928535	0.86[CEU][hapmap];0.86[YRI][hapmap]
rs6475226	0.86[CEU][hapmap];0.82[JPT][hapmap];0.81[YRI][hapmap]
rs6475228	0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs7022259	0.86[CEU][hapmap]
rs7027894	0.80[ASN][1000 genomes]
rs7039094	0.91[CEU][hapmap]
rs7042143	0.82[CHB][hapmap];0.86[JPT][hapmap];0.81[YRI][hapmap];0.81[ASN][1000 genomes]
rs7042159	0.82[CHB][hapmap];0.86[JPT][hapmap];0.86[YRI][hapmap];0.83[AFR][1000 genomes]
rs7466047	0.90[CEU][hapmap];0.82[CHB][hapmap]
rs7466067	0.90[CEU][hapmap]
rs7849918	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs951226	0.95[AFR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491807	chr9:18243672-19009770	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv525659	chr9:18288212-19009041	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1019127	chr9:18288271-18996288	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv1029449	chr9:18414752-18829127	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
5	nsv540077	chr9:18414752-18829127	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
6	nsv1030931	chr9:18414752-18903530	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
7	nsv892690	chr9:18485434-18592374	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
8	nsv428536	chr9:18512807-18667760	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
9	nsv892691	chr9:18519699-18805483	Weak transcription Enhancers Strong transcription Flanking Active TSS Active 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	4 gene(s)	inside rSNPs	diseases
10	nsv892692	chr9:18519699-19045502	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
11	nsv892693	chr9:18541710-18584860	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
12	esv2430566	chr9:18574479-18575902	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:18564400-18591800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:18566800-18579600	Weak transcription	HSMMtube	muscle
3	chr9:18567000-18579600	Weak transcription	HUVEC	blood vessel
4	chr9:18567800-18578000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr9:18569600-18575600	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr9:18569600-18580200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr9:18569800-18601000	Weak transcription	NHLF	lung
8	chr9:18570200-18583200	Weak transcription	Fetal Stomach	stomach
9	chr9:18570200-18591800	Weak transcription	Aorta	Aorta
10	chr9:18571000-18575400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr9:18571800-18579200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr9:18573200-18579000	Strong transcription	HSMM	muscle
13	chr9:18573800-18575400	Strong transcription	NH-A	brain
14	chr9:18574000-18575000	Strong transcription	NHDF-Ad	bronchial
15	chr9:18574000-18575200	Strong transcription	Muscle Satellite Cultured Cells	--
16	chr9:18574400-18581600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr9:18574600-18576200	Weak transcription	Osteobl	bone

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