Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10036337	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10043080	1.00[CHB][hapmap];0.83[CHD][hapmap]
rs10060241	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10060250	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10071854	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10074010	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10080163	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12109171	1.00[CHB][hapmap];0.83[CHD][hapmap]
rs13356315	0.93[ASN][1000 genomes]
rs1358224	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17345486	1.00[ASN][1000 genomes]
rs17403118	1.00[ASN][1000 genomes]
rs34279532	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3850728	1.00[ASN][1000 genomes]
rs56819255	0.93[ASN][1000 genomes]
rs60808813	0.93[ASN][1000 genomes]
rs62378112	0.93[ASN][1000 genomes]
rs62380274	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73262789	0.93[ASN][1000 genomes]
rs7707471	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9327047	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882757	chr5:116810010-117042759	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv830458	chr5:116831747-117003041	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv1016664	chr5:116888074-117181273	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1019332	chr5:116888074-117248632	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:116987800-116989200	Enhancers	HSMM	muscle
2	chr5:116988000-116989000	Enhancers	Muscle Satellite Cultured Cells	--
3	chr5:116988400-116989400	Enhancers	Fetal Heart	heart
4	chr5:116988600-116989000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr5:116988800-116993200	Weak transcription	Fetal Brain Female	brain

Quick Search: