Variant report

Variant	rs11006714
Chromosome Location	chr10:28075294-28075295
allele	C/T
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:51)

rs_ID	r²[population]
rs10430558	1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10430568	1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1055192	0.83[ASN][1000 genomes]
rs10826346	1.00[CHB][hapmap];0.83[ASN][1000 genomes]
rs10826349	0.86[EUR][1000 genomes]
rs11006694	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs11006698	0.83[ASN][1000 genomes]
rs11006699	0.83[ASN][1000 genomes]
rs11006700	0.83[ASN][1000 genomes]
rs11006703	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11006704	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11006705	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11006707	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11006708	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11006715	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11006717	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11006719	0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11006720	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11006723	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11006725	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11006728	0.91[CHB][hapmap];1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11006733	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs11015948	0.92[CHB][hapmap];0.97[CHD][hapmap]
rs11015980	1.00[CHB][hapmap]
rs11015981	1.00[CHB][hapmap]
rs11814132	1.00[TSI][hapmap]
rs12218027	1.00[CHB][hapmap]
rs12264856	1.00[CHB][hapmap];0.94[CHD][hapmap]
rs2065689	0.92[CHB][hapmap]
rs2225713	1.00[TSI][hapmap]
rs35242712	1.00[AFR][1000 genomes]
rs35472668	1.00[AFR][1000 genomes]
rs3737184	0.92[CHB][hapmap];1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7071046	0.90[ASN][1000 genomes]
rs7077315	1.00[TSI][hapmap]
rs7077784	0.92[CHB][hapmap]
rs7097374	1.00[TSI][hapmap]
rs7100957	1.00[TSI][hapmap]
rs72631839	0.84[ASN][1000 genomes]
rs72631840	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72631841	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72631842	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72631843	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72631844	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72631845	1.00[EUR][1000 genomes]
rs72631846	0.84[AMR][1000 genomes]
rs7358151	1.00[CHB][hapmap];1.00[TSI][hapmap]
rs7893159	1.00[TSI][hapmap]
rs7899995	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs8181307	1.00[CHB][hapmap]
rs952404	0.92[CHB][hapmap];1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831813	chr10:28017606-28200651	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv917149	chr10:28018919-28688694	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv971859	chr10:28070066-28271252	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr10:28074000-28080200	Weak transcription	Aorta	Aorta

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