Variant report

Variant	rs9367336
Chromosome Location	chr6:48890685-48890686
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs11759831	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1546859	0.89[AMR][1000 genomes]
rs16878440	0.96[AMR][1000 genomes]
rs2092143	0.89[AMR][1000 genomes]
rs2092144	0.89[AMR][1000 genomes]
rs4431432	0.89[AMR][1000 genomes]
rs4506041	0.89[AMR][1000 genomes]
rs56184668	0.83[AMR][1000 genomes]
rs6906833	0.89[AMR][1000 genomes]
rs6931219	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6934834	0.89[AMR][1000 genomes]
rs72862092	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72862093	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72863619	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs72863636	0.89[AMR][1000 genomes]
rs72863637	0.89[AMR][1000 genomes]
rs72863638	0.89[AMR][1000 genomes]
rs72863639	0.89[AMR][1000 genomes]
rs72863640	0.89[AMR][1000 genomes]
rs72863649	0.89[AMR][1000 genomes]
rs72863654	0.83[AMR][1000 genomes]
rs72863660	0.80[AMR][1000 genomes]
rs72863679	0.83[AMR][1000 genomes]
rs72863681	0.80[AMR][1000 genomes]
rs742116	0.82[EUR][1000 genomes]
rs7740349	0.86[AMR][1000 genomes]
rs7758514	0.89[AMR][1000 genomes]
rs7767596	0.89[AMR][1000 genomes]
rs7775809	0.89[AMR][1000 genomes]
rs9349460	0.89[AMR][1000 genomes]
rs9349461	0.89[AMR][1000 genomes]
rs9349462	0.83[AMR][1000 genomes]
rs9349464	0.89[AMR][1000 genomes]
rs9357589	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9357590	0.86[AMR][1000 genomes]
rs9357592	0.89[AMR][1000 genomes]
rs9367341	0.82[AMR][1000 genomes]
rs9369829	0.89[AMR][1000 genomes]
rs9369830	0.89[AMR][1000 genomes]
rs9369831	0.89[AMR][1000 genomes]
rs9369832	0.89[AMR][1000 genomes]
rs9369833	0.89[AMR][1000 genomes]
rs9369834	0.89[AMR][1000 genomes]
rs9369837	0.89[AMR][1000 genomes]
rs9369838	0.89[AMR][1000 genomes]
rs9381709	0.89[AMR][1000 genomes]
rs9381712	0.89[AMR][1000 genomes]
rs9381716	0.89[AMR][1000 genomes]
rs9395426	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9395429	0.89[AMR][1000 genomes]
rs9395430	0.89[AMR][1000 genomes]
rs9395432	0.89[AMR][1000 genomes]
rs9395434	0.89[AMR][1000 genomes]
rs9395435	0.89[AMR][1000 genomes]
rs9395438	0.89[AMR][1000 genomes]
rs9395440	0.89[AMR][1000 genomes]
rs9395441	0.89[AMR][1000 genomes]
rs9395443	0.96[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949690	chr6:48595821-49289855	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv603037	chr6:48804862-48995221	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:48832200-48944000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:48887800-48892200	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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