Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:79808364..79810054-chr14:79814203..79817029,2	K562	blood:

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10146833	0.92[CEU][hapmap];0.83[CHB][hapmap];0.84[TSI][hapmap];0.89[EUR][1000 genomes]
rs10498537	0.88[CEU][hapmap];0.83[CHB][hapmap];0.80[TSI][hapmap];0.84[EUR][1000 genomes]
rs11625994	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12432262	0.90[CHD][hapmap]
rs12590794	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12882688	0.85[CHD][hapmap]
rs12888473	0.89[EUR][1000 genomes]
rs12888937	0.81[AFR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12889183	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12889273	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12894140	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12895906	0.84[CEU][hapmap];0.83[CHB][hapmap];0.83[EUR][1000 genomes]
rs12896073	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1868635	0.90[CHD][hapmap]
rs2122434	0.93[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.82[GIH][hapmap];0.90[JPT][hapmap];0.86[LWK][hapmap];0.89[TSI][hapmap];0.93[YRI][hapmap];0.82[AFR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2167150	0.92[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4903845	0.91[EUR][1000 genomes]
rs4903846	0.84[EUR][1000 genomes]
rs6574506	0.90[EUR][1000 genomes]
rs7161543	0.81[CHD][hapmap]
rs7492987	1.00[CEU][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs8006756	0.88[CEU][hapmap];0.83[CHB][hapmap];0.84[EUR][1000 genomes]
rs8008332	0.85[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	nsv931412	chr14:79420297-79928269	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv902110	chr14:79624492-79998294	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv530072	chr14:79769657-79928269	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv902111	chr14:79807197-79890677	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs17598373	FLVCR2	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79792200-79825600	Weak transcription	Aorta	Aorta

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