Variant report

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

rs_ID	r²[population]
rs10801208	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10801209	0.80[AFR][1000 genomes]
rs10801211	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10801212	0.92[AFR][1000 genomes]
rs10801213	0.92[AFR][1000 genomes]
rs10921397	0.83[AFR][1000 genomes]
rs10921400	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12022959	0.95[AFR][1000 genomes]
rs12028044	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1410402	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1556901	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16835709	0.81[ASN][1000 genomes]
rs1887726	0.85[AFR][1000 genomes]
rs2031831	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2370444	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs2370445	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs34745330	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4495677	0.83[AFR][1000 genomes]
rs4657876	0.90[AFR][1000 genomes]
rs6684853	0.80[AFR][1000 genomes]
rs7413068	0.83[AFR][1000 genomes]
rs7547559	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7553889	0.83[AFR][1000 genomes]
rs958958	0.92[AFR][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	nsv1008266	chr1:193550185-194481053	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv3372415	chr1:193612172-193988265	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr1:193617800-193618400	Active TSS	Fetal Heart	heart

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