Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:32510736..32513682-chr11:32515069..32517545,2	K562	blood:

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10767940	0.87[ASN][1000 genomes]
rs10767942	0.98[ASN][1000 genomes]
rs10835921	0.83[EUR][1000 genomes]
rs10835928	0.93[ASN][1000 genomes]
rs10835930	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10835932	0.88[ASN][1000 genomes]
rs11031820	0.87[ASN][1000 genomes]
rs11031822	0.98[ASN][1000 genomes]
rs11031830	0.98[ASN][1000 genomes]
rs12222697	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12224136	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3858449	0.85[CEU][hapmap]
rs3890511	0.98[ASN][1000 genomes]
rs5030141	0.85[CEU][hapmap]
rs60599105	0.87[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs61891673	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs61891678	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7114294	0.86[ASN][1000 genomes]
rs7130245	0.98[ASN][1000 genomes]
rs7483925	0.89[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	nsv832108	chr11:32395937-32560583	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs10835931	CSTF3	cis	cerebellum	SCAN
rs10835931	CD59	cis	cerebellum	SCAN

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32514400-32516600	Enhancers	Dnd41	blood
2	chr11:32515000-32516400	Weak transcription	Ovary	ovary

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