Variant report

Variant	rs11721706
Chromosome Location	chr4:16281681-16281682
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10489057	0.94[EUR][1000 genomes]
rs11722358	0.94[EUR][1000 genomes]
rs11722711	0.82[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs11735255	0.86[CEU][hapmap];0.88[GIH][hapmap];1.00[LWK][hapmap];0.94[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11735313	0.91[EUR][1000 genomes]
rs11736850	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11945394	0.94[EUR][1000 genomes]
rs1472572	0.93[EUR][1000 genomes]
rs16893218	0.92[EUR][1000 genomes]
rs16893239	0.95[EUR][1000 genomes]
rs16893257	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs16893316	0.86[CEU][hapmap];0.88[GIH][hapmap];0.83[LWK][hapmap];0.94[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs16893388	0.93[EUR][1000 genomes]
rs16893404	0.81[GIH][hapmap];0.88[MEX][hapmap];0.95[TSI][hapmap];0.94[EUR][1000 genomes]
rs16893419	0.91[EUR][1000 genomes]
rs1860821	0.94[EUR][1000 genomes]
rs2041540	0.94[EUR][1000 genomes]
rs2072437	0.94[EUR][1000 genomes]
rs28566142	0.93[EUR][1000 genomes]
rs28650994	0.93[EUR][1000 genomes]
rs28659920	0.94[EUR][1000 genomes]
rs2940	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs41447446	0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs57049226	0.80[ASN][1000 genomes]
rs57653099	0.82[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs57773089	0.82[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs59486353	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs59502099	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs60788991	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6449231	0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs67922017	0.92[EUR][1000 genomes]
rs6815561	0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6828457	0.81[GIH][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap]
rs6830484	0.91[EUR][1000 genomes]
rs6830697	0.92[EUR][1000 genomes]
rs6844412	0.95[EUR][1000 genomes]
rs6846948	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73118069	0.94[EUR][1000 genomes]
rs73118071	0.94[EUR][1000 genomes]
rs73121857	0.94[EUR][1000 genomes]
rs73127513	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73127519	0.82[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs73127521	0.82[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs73127531	0.94[EUR][1000 genomes]
rs73127547	0.93[EUR][1000 genomes]
rs73127555	0.84[EUR][1000 genomes]
rs73798733	0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7660573	0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7673330	0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7689789	0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1004821	chr4:16055996-16830629	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv537046	chr4:16055996-16830629	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv537047	chr4:16182060-16375787	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv537048	chr4:16226406-16375787	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 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	chr4:16279200-16282400	Weak transcription	Aorta	Aorta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links