Variant report

Variant	rs17221418
Chromosome Location	chr6:56064305-56064306
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 73 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10484705	1.00[CEU][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10484706	1.00[CEU][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10484707	1.00[CEU][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10484708	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10807509	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs12154070	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12190240	1.00[CEU][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12193215	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12193262	1.00[ASN][1000 genomes]
rs12193617	1.00[CEU][hapmap]
rs12194691	1.00[ASN][1000 genomes]
rs12195034	1.00[CEU][hapmap];1.00[ASN][1000 genomes]
rs12196208	1.00[CEU][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12196632	1.00[CEU][hapmap];1.00[ASN][1000 genomes]
rs12197715	1.00[CEU][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12198686	1.00[CEU][hapmap]
rs12201639	1.00[CEU][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12202221	1.00[CEU][hapmap];1.00[ASN][1000 genomes]
rs12202885	1.00[CEU][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12202972	1.00[CEU][hapmap];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12203971	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12204894	1.00[CEU][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12206360	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12206617	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12207093	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12207333	1.00[CEU][hapmap];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12207447	1.00[CEU][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12207650	1.00[CEU][hapmap];1.00[ASN][1000 genomes]
rs12208804	1.00[CEU][hapmap];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12209422	1.00[ASN][1000 genomes]
rs12209452	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12214023	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12214985	1.00[ASN][1000 genomes]
rs12216230	1.00[ASN][1000 genomes]
rs17222493	1.00[ASN][1000 genomes]
rs17821163	1.00[CEU][hapmap];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1925146	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1925150	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1925151	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1925168	1.00[CEU][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1925183	1.00[CEU][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764061	1.00[CEU][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2840999	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28452747	1.00[ASN][1000 genomes]
rs4326238	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61465988	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61524954	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62411454	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62411866	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62411869	1.00[ASN][1000 genomes]
rs62411870	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62412798	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62412802	1.00[ASN][1000 genomes]
rs62413463	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62413464	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62413466	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62413468	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62413482	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62413546	1.00[ASN][1000 genomes]
rs62413548	0.95[EUR][1000 genomes]
rs62413549	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62413552	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62413553	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62413554	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62413555	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6459150	1.00[ASN][1000 genomes]
rs7742633	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7771018	1.00[ASN][1000 genomes]
rs885631	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs990188	1.00[ASN][1000 genomes]
rs990189	1.00[ASN][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:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:56060000-56064400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr6:56062000-56064800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr6:56064000-56090800	Weak transcription	Fetal Lung	lung

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