Variant report

Variant	rs340934
Chromosome Location	chr9:6081804-6081805
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 86 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs10739084	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10975412	0.94[EUR][1000 genomes]
rs10975413	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10975416	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1330124	0.91[CEU][hapmap];0.82[GIH][hapmap];0.90[TSI][hapmap];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1332291	0.81[EUR][1000 genomes]
rs1332292	0.88[EUR][1000 genomes]
rs1537285	0.88[EUR][1000 genomes]
rs1556470	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1591044	0.88[EUR][1000 genomes]
rs168168	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1755531	0.88[EUR][1000 genomes]
rs189348	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1970089	0.88[EUR][1000 genomes]
rs2150969	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs340887	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs340893	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs340894	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs340896	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs340901	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs340902	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs340903	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs340904	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs340905	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs340906	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs340918	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs340919	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs340921	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs340922	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs340923	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs340924	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs340925	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs340926	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs340933	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs340935	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs343475	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs343476	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs343479	0.97[EUR][1000 genomes]
rs343489	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs343490	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs343491	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs343495	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs343496	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs369996	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs371165	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs371454	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs372560	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs374672	0.88[EUR][1000 genomes]
rs375560	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs376690	0.88[EUR][1000 genomes]
rs378952	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs380568	0.91[CEU][hapmap];0.83[GIH][hapmap];0.90[TSI][hapmap];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs380888	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs390158	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs393556	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs397505	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs397916	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs398561	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs399834	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs401731	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs401834	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs420445	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs425489	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs437389	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs441616	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs442851	0.88[EUR][1000 genomes]
rs443175	0.88[EUR][1000 genomes]
rs451974	0.88[EUR][1000 genomes]
rs4742151	0.92[ASN][1000 genomes]
rs503384	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs503507	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs531759	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62558390	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs639247	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs694796	0.88[EUR][1000 genomes]
rs695013	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs821164	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9407312	0.88[EUR][1000 genomes]
rs9408638	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs974936	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 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

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs340934	SMARCA2	cis	parietal	SCAN
rs340934	C9orf68	cis	cerebellum	SCAN
rs340934	JAK2	cis	cerebellum	SCAN
rs340934	C9orf70	cis	parietal	SCAN

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6081400-6084000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr9:6081600-6087200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr9:6081800-6082000	Enhancers	ES-I3 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links