Variant report

Variant	rs12193215
Chromosome Location	chr6:56066674-56066675
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10484705	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10484706	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10484707	1.00[EUR][1000 genomes]
rs10484708	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10807509	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12154070	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12190240	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12196208	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12197715	0.95[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12201639	0.98[EUR][1000 genomes]
rs12202885	0.98[EUR][1000 genomes]
rs12202972	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12203971	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12204894	0.98[EUR][1000 genomes]
rs12206360	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12206617	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12207093	0.98[EUR][1000 genomes]
rs12207333	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12207447	0.95[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12208804	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12214023	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17221418	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17222493	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs17821163	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1925146	0.88[EUR][1000 genomes]
rs1925150	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1925151	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1925168	0.80[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs1925183	0.98[EUR][1000 genomes]
rs2764061	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2840999	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4326238	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61465988	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61524954	1.00[EUR][1000 genomes]
rs62411454	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62411866	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62411869	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs62411870	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62412798	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62413463	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62413464	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62413466	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62413468	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62413482	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62413546	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs62413548	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62413549	0.95[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62413552	0.98[EUR][1000 genomes]
rs62413553	0.98[EUR][1000 genomes]
rs62413554	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62413555	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7742633	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7771018	0.82[AMR][1000 genomes]
rs885631	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs990188	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs990189	1.00[AFR][1000 genomes];0.95[AMR][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	nsv1034037	chr6:55222409-56069600	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv885911	chr6:55789704-56143231	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:56064000-56090800	Weak transcription	Fetal Lung	lung
2	chr6:56065200-56069000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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