Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1203340	0.95[ASN][1000 genomes]
rs1203341	0.95[ASN][1000 genomes]
rs1203342	0.95[ASN][1000 genomes]
rs1203343	0.95[ASN][1000 genomes]
rs1203344	0.94[ASN][1000 genomes]
rs1203345	0.94[ASN][1000 genomes]
rs1203346	0.94[ASN][1000 genomes]
rs1203347	0.94[ASN][1000 genomes]
rs1203348	0.94[ASN][1000 genomes]
rs12526873	0.87[ASN][1000 genomes]
rs1933759	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1933764	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1933765	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1933766	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1933768	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2326916	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2876084	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4897429	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6569688	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6940599	0.87[ASN][1000 genomes]
rs766966	0.94[ASN][1000 genomes]
rs766967	0.95[ASN][1000 genomes]
rs9321230	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9375731	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9388802	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[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	nsv533971	chr6:130490694-131172051	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:130855200-130858200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr6:130857800-130858200	Weak transcription	Primary T cells from cord blood	blood
3	chr6:130857800-130859200	Enhancers	Primary T cells fromperipheralblood	blood
4	chr6:130857800-130859200	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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