Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10734050	0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10734051	0.92[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs10741040	0.83[ASN][1000 genomes]
rs10741042	0.89[AFR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10764447	0.94[AFR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10828605	0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10828606	0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10828616	0.95[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs10828617	0.94[AFR][1000 genomes]
rs11013865	0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1325991	0.83[ASN][1000 genomes]
rs16917217	0.83[ASN][1000 genomes]
rs17539088	0.83[ASN][1000 genomes]
rs1926028	0.83[ASN][1000 genomes]
rs61839222	0.83[ASN][1000 genomes]
rs61839226	0.95[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs7072365	0.94[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs7085825	0.94[AFR][1000 genomes]
rs7099729	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7901058	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7907743	0.80[ASN][1000 genomes]
rs7908718	0.95[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7911051	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7920123	0.82[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046458	chr10:18629603-18683860	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7910898	CACNB2	cis	thalamus	BrainEAC

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:18639600-18661400	Weak transcription	Aorta	Aorta
2	chr10:18652400-18667400	Weak transcription	Left Ventricle	heart
3	chr10:18658000-18664800	Weak transcription	Fetal Heart	heart
4	chr10:18659400-18676000	Weak transcription	Right Ventricle	heart

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