Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:108564779..108567807-chr5:108568238..108570638,3	K562	blood:

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

rs_ID	r²[population]
rs11743213	0.82[EUR][1000 genomes]
rs12515174	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12520021	0.81[ASN][1000 genomes]
rs12522058	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12522411	0.81[ASN][1000 genomes]
rs1363214	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1422003	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17473588	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17473831	0.82[EUR][1000 genomes]
rs4645374	0.81[ASN][1000 genomes]
rs57400924	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs60496657	0.81[ASN][1000 genomes]
rs62376831	0.88[EUR][1000 genomes]
rs62376832	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6864796	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6866668	0.81[ASN][1000 genomes]
rs6877495	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6881141	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6884332	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6899020	0.81[ASN][1000 genomes]
rs7700949	0.81[ASN][1000 genomes]
rs7718897	0.80[ASN][1000 genomes]
rs7720237	0.81[ASN][1000 genomes]
rs7727900	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9968753	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];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	nsv1027163	chr5:108445447-108839913	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv599338	chr5:108528729-108675737	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:108567400-108570200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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