Variant report

Variant	rs4381616
Chromosome Location	chr16:80030936-80030937
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr16:80003227..80006077-chr16:80028568..80030981,2	K562	blood:
2	chr16:80028844..80032555-chr16:80035015..80037788,3	K562	blood:
3	chr16:80030381..80031931-chr16:80117976..80119153,11	MCF-7	breast:

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs11645608	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11645885	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11646780	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11647839	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12149105	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12149738	0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12921341	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12923727	0.92[EUR][1000 genomes]
rs12923732	0.92[EUR][1000 genomes]
rs12930889	0.90[EUR][1000 genomes]
rs28425168	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35244260	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3924082	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs3936188	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4073088	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4073089	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4076249	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4076250	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4076251	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4341754	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4426358	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4439776	0.89[EUR][1000 genomes]
rs4445914	0.87[EUR][1000 genomes]
rs4485384	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4490014	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4505341	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4611478	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4888064	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6564723	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs8053769	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs8057036	0.89[EUR][1000 genomes]
rs8063712	0.86[EUR][1000 genomes]
rs9921198	0.85[EUR][1000 genomes]
rs9923757	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9923939	0.89[EUR][1000 genomes]
rs9923943	0.89[EUR][1000 genomes]
rs9924079	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9924359	0.88[EUR][1000 genomes]
rs9924378	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9926410	0.89[EUR][1000 genomes]
rs9927433	0.90[EUR][1000 genomes]
rs9929759	0.94[EUR][1000 genomes]
rs9929923	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9930005	0.89[EUR][1000 genomes]
rs9931548	0.88[EUR][1000 genomes]
rs9932265	0.88[EUR][1000 genomes]
rs9932617	0.87[EUR][1000 genomes]
rs9934311	0.89[EUR][1000 genomes]
rs9935292	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9936732	0.88[EUR][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	nsv573285	chr16:79158182-80127326	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv573294	chr16:80005642-80131944	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:80028200-80040000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr16:80030400-80031800	Enhancers	K562	blood
3	chr16:80030800-80031200	Weak transcription	Aorta	Aorta

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