Variant report

Variant	rs9364714
Chromosome Location	chr6:164466872-164466873
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:164465175..164467535-chr6:164468011..164470571,2	MCF-7	breast:
2	chr6:164457700..164459500-chr6:164464976..164467950,2	K562	blood:

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs10455794	0.87[ASN][1000 genomes]
rs10755598	0.87[ASN][1000 genomes]
rs10806788	0.87[ASN][1000 genomes]
rs10806789	0.87[ASN][1000 genomes]
rs10945948	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10945949	0.87[ASN][1000 genomes]
rs10945950	0.87[ASN][1000 genomes]
rs10945951	0.89[ASN][1000 genomes]
rs12055516	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs12055870	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs12175904	0.89[ASN][1000 genomes]
rs12200189	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12204824	0.89[ASN][1000 genomes]
rs12208775	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12208802	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12216473	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12216523	0.89[ASN][1000 genomes]
rs12527242	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12527246	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs12527249	0.85[ASN][1000 genomes]
rs12530262	0.87[ASN][1000 genomes]
rs13212664	0.87[ASN][1000 genomes]
rs1436856	0.87[ASN][1000 genomes]
rs1436857	0.87[ASN][1000 genomes]
rs1436858	0.87[ASN][1000 genomes]
rs1436859	0.87[ASN][1000 genomes]
rs1436860	0.87[ASN][1000 genomes]
rs1898308	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2033705	1.00[YRI][hapmap]
rs205996	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs206688	0.89[ASN][1000 genomes]
rs34312142	0.89[ASN][1000 genomes]
rs35317099	0.87[ASN][1000 genomes]
rs366572	0.89[ASN][1000 genomes]
rs368303	0.87[ASN][1000 genomes]
rs369635	0.89[ASN][1000 genomes]
rs377662	0.89[ASN][1000 genomes]
rs379046	0.89[ASN][1000 genomes]
rs379084	0.89[ASN][1000 genomes]
rs380640	0.89[ASN][1000 genomes]
rs383861	0.89[ASN][1000 genomes]
rs384090	0.89[ASN][1000 genomes]
rs386112	0.89[ASN][1000 genomes]
rs390097	0.89[ASN][1000 genomes]
rs390662	0.89[ASN][1000 genomes]
rs392649	0.89[ASN][1000 genomes]
rs396207	0.87[ASN][1000 genomes]
rs407411	0.88[ASN][1000 genomes]
rs411505	0.89[ASN][1000 genomes]
rs412544	0.89[ASN][1000 genomes]
rs412553	0.89[ASN][1000 genomes]
rs414708	0.89[ASN][1000 genomes]
rs418309	0.89[ASN][1000 genomes]
rs418319	0.89[ASN][1000 genomes]
rs419927	0.89[ASN][1000 genomes]
rs422371	0.89[ASN][1000 genomes]
rs422805	0.89[ASN][1000 genomes]
rs429361	0.89[ASN][1000 genomes]
rs445855	0.87[ASN][1000 genomes]
rs71569438	0.85[ASN][1000 genomes]
rs71569439	0.85[ASN][1000 genomes]
rs9346989	0.89[ASN][1000 genomes]
rs9346990	0.89[ASN][1000 genomes]
rs9346991	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9347815	0.88[ASN][1000 genomes]
rs9347816	0.89[ASN][1000 genomes]
rs9347817	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9355457	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9355459	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9364715	0.89[ASN][1000 genomes]
rs9365649	0.86[ASN][1000 genomes]
rs9365652	0.87[ASN][1000 genomes]
rs9365656	0.84[ASN][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	nsv1018860	chr6:163939347-164532579	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription 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 target site	14 gene(s)	inside rSNPs	diseases
2	nsv538526	chr6:163939347-164532579	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv1026707	chr6:164188210-164749206	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv538527	chr6:164188210-164749206	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv1019703	chr6:164424683-164488780	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1029952	chr6:164463355-165268911	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:164466600-164470400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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