Variant report

Variant	rs968826
Chromosome Location	chr8:69565806-69565807
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10101569	0.86[ASN][1000 genomes]
rs10957442	0.97[ASN][1000 genomes]
rs1116986	0.85[ASN][1000 genomes]
rs11780358	0.82[ASN][1000 genomes]
rs11780828	0.89[ASN][1000 genomes]
rs11781537	0.86[ASN][1000 genomes]
rs11781575	0.85[ASN][1000 genomes]
rs12675138	0.84[ASN][1000 genomes]
rs12681248	0.84[ASN][1000 genomes]
rs12681467	0.86[ASN][1000 genomes]
rs13275978	0.86[ASN][1000 genomes]
rs1583423	0.82[ASN][1000 genomes]
rs16919105	0.86[ASN][1000 genomes]
rs1865440	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1865441	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1865443	0.96[ASN][1000 genomes]
rs1897906	0.97[ASN][1000 genomes]
rs1991960	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2082723	0.85[ASN][1000 genomes]
rs2196255	0.90[ASN][1000 genomes]
rs2196256	0.90[ASN][1000 genomes]
rs2890437	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62520961	0.90[ASN][1000 genomes]
rs62520962	0.83[ASN][1000 genomes]
rs62520966	0.86[ASN][1000 genomes]
rs6982247	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6982315	0.83[ASN][1000 genomes]
rs6982710	0.96[ASN][1000 genomes]
rs7007623	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7464474	0.86[ASN][1000 genomes]
rs766871	0.85[ASN][1000 genomes]
rs7812470	0.85[ASN][1000 genomes]
rs959451	0.86[ASN][1000 genomes]
rs961465	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][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	nsv948687	chr8:69041121-69642540	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv890985	chr8:69532253-69586034	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv831349	chr8:69555461-69733515	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv972529	chr8:69561897-69568157	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:69545200-69572800	Weak transcription	Aorta	Aorta

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