Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:46313038..46315945-chr3:46324177..46326362,2	K562	blood:

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs13065351	0.81[EUR][1000 genomes]
rs13068145	0.81[EUR][1000 genomes]
rs13068271	0.81[EUR][1000 genomes]
rs13071469	0.81[EUR][1000 genomes]
rs13077302	0.81[EUR][1000 genomes]
rs13078564	0.81[EUR][1000 genomes]
rs13093063	0.81[EUR][1000 genomes]
rs13100243	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17284138	0.81[EUR][1000 genomes]
rs17284187	0.81[EUR][1000 genomes]
rs28677778	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs34073838	0.81[EUR][1000 genomes]
rs35117954	0.81[EUR][1000 genomes]
rs35203745	0.80[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs35218998	0.81[EUR][1000 genomes]
rs35373513	0.81[EUR][1000 genomes]
rs35511592	0.81[EUR][1000 genomes]
rs35646896	0.81[EUR][1000 genomes]
rs36078103	0.81[EUR][1000 genomes]
rs4473594	0.81[EUR][1000 genomes]
rs4987053	0.81[AMR][1000 genomes]
rs6793370	0.80[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs71327047	0.81[EUR][1000 genomes]
rs71622511	0.81[AMR][1000 genomes]
rs7649905	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9810242	0.80[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9872023	0.81[EUR][1000 genomes]
rs9882616	0.81[EUR][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	nsv876734	chr3:45725031-46468467	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv498008	chr3:45733423-46319401	Strong transcription Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46312000-46317600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
2	chr3:46312600-46317600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr3:46312600-46318000	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr3:46312600-46318200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr3:46315400-46315800	Enhancers	Primary monocytes fromperipheralblood	blood

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