Variant report

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

rs_ID	r²[population]
rs10485155	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1323323	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17062751	1.00[ASN][1000 genomes]
rs17062755	1.00[ASN][1000 genomes]
rs17062767	1.00[ASN][1000 genomes]
rs17062783	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17062790	1.00[ASN][1000 genomes]
rs17062815	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17062821	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17062832	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57857547	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58009634	0.90[ASN][1000 genomes]
rs59489488	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60294591	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6907624	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73773668	1.00[ASN][1000 genomes]
rs73776704	0.90[ASN][1000 genomes]
rs73776712	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs73776716	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73776717	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73776723	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7746823	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7753057	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9493730	1.00[EUR][1000 genomes];1.00[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	nsv830812	chr6:133993897-134165407	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:134063000-134069800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr6:134063000-134070800	Weak transcription	Right Atrium	heart
3	chr6:134063000-134073000	Weak transcription	Fetal Kidney	kidney
4	chr6:134063600-134068800	Weak transcription	Fetal Lung	lung
5	chr6:134065600-134068600	Weak transcription	Fetal Stomach	stomach
6	chr6:134065800-134070000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr6:134067200-134072800	Weak transcription	Osteobl	bone
8	chr6:134067600-134075000	Weak transcription	Stomach Mucosa	stomach
9	chr6:134067800-134068600	Active TSS	K562	blood
10	chr6:134068000-134073000	Weak transcription	A549	lung

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