Variant report

Variant	rs340895
Chromosome Location	chr9:6104244-6104245
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10739084	0.88[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs1332292	0.83[EUR][1000 genomes]
rs1537285	0.83[EUR][1000 genomes]
rs1556470	0.81[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs1591044	0.83[EUR][1000 genomes]
rs168168	0.85[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs1755531	0.83[EUR][1000 genomes]
rs1970089	0.83[EUR][1000 genomes]
rs2150969	0.86[EUR][1000 genomes]
rs340887	0.86[EUR][1000 genomes]
rs340893	0.90[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs340894	0.90[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs340896	0.90[AFR][1000 genomes];0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs340901	0.86[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs340902	0.87[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs340903	0.86[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs340904	0.88[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs340905	0.89[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs340906	0.90[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs340918	0.84[EUR][1000 genomes]
rs340919	0.84[EUR][1000 genomes]
rs340921	0.86[EUR][1000 genomes]
rs340922	0.81[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs340923	0.84[EUR][1000 genomes]
rs340924	0.84[EUR][1000 genomes]
rs340925	0.81[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs340926	0.87[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs340933	0.87[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs369996	0.86[EUR][1000 genomes]
rs371165	0.86[EUR][1000 genomes]
rs372560	0.85[EUR][1000 genomes]
rs374672	0.83[EUR][1000 genomes]
rs375560	0.83[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs376690	0.83[EUR][1000 genomes]
rs380888	0.86[EUR][1000 genomes]
rs390158	0.86[EUR][1000 genomes]
rs397916	0.86[EUR][1000 genomes]
rs398561	0.88[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs399834	0.87[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs401731	0.85[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs420445	0.86[EUR][1000 genomes]
rs425489	0.86[EUR][1000 genomes]
rs437389	0.91[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs441616	0.83[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs442851	0.83[EUR][1000 genomes]
rs443175	0.83[EUR][1000 genomes]
rs503384	0.86[EUR][1000 genomes]
rs503507	0.86[EUR][1000 genomes]
rs531759	0.86[EUR][1000 genomes]
rs639247	0.86[EUR][1000 genomes]
rs694796	0.83[EUR][1000 genomes]
rs695013	0.81[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs821164	0.84[EUR][1000 genomes]
rs9407312	0.83[EUR][1000 genomes]
rs9408638	0.90[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs974936	0.81[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948847	chr9:5712626-6417677	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv1031086	chr9:5806949-6630686	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	nsv539967	chr9:5806949-6630686	Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
4	nsv1015450	chr9:5915640-6114652	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
5	nsv613205	chr9:6032924-6332901	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv916394	chr9:6055497-6322471	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	esv2761482	chr9:6084602-6134787	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv892157	chr9:6093790-6322415	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv933124	chr9:6099101-6644738	Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
10	nsv831496	chr9:6101763-6285088	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6098800-6105200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr9:6099200-6106600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr9:6101600-6104800	Enhancers	NHEK	skin
4	chr9:6101600-6105400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr9:6101600-6107200	Enhancers	HMEC	breast
6	chr9:6101800-6105400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr9:6102000-6106400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr9:6103000-6106800	Weak transcription	HUVEC	blood vessel
9	chr9:6103000-6107000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr9:6103000-6108600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr9:6103400-6106400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr9:6103400-6106800	Weak transcription	NHDF-Ad	bronchial
13	chr9:6103800-6106800	Enhancers	Hela-S3	cervix

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