Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10462093	0.83[ASN][1000 genomes]
rs10805698	0.83[ASN][1000 genomes]
rs12518235	0.83[ASN][1000 genomes]
rs12520275	0.83[ASN][1000 genomes]
rs16902220	0.83[ASN][1000 genomes]
rs2337953	0.83[ASN][1000 genomes]
rs61630137	0.83[ASN][1000 genomes]
rs61734825	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61735895	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs62367670	0.83[ASN][1000 genomes]
rs62367671	0.83[ASN][1000 genomes]
rs62367672	0.83[ASN][1000 genomes]
rs62370584	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62370618	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62371977	0.96[EUR][1000 genomes]
rs62372026	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62372037	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73090063	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73107077	0.86[ASN][1000 genomes]
rs7442769	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7443189	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7444228	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[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	nsv831915	chr1:173268424-173482157	Flanking Active TSS Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:173264600-173298200	Weak transcription	HSMMtube	muscle
2	chr1:173285000-173300200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr1:173288200-173301000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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