Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:34819581..34822013-chr3:34831839..34833484,2	K562	blood:
2	chr3:34815559..34817841-chr3:34819019..34821368,2	K562	blood:

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1522967	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs4449263	0.82[AMR][1000 genomes]
rs510111	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs522543	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs528377	0.82[AFR][1000 genomes]
rs548933	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs549416	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs558254	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs559478	0.82[AFR][1000 genomes]
rs589956	0.82[AFR][1000 genomes]
rs600767	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs603928	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs605758	0.82[AFR][1000 genomes]
rs608250	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs615403	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs651154	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs652932	0.80[AFR][1000 genomes]
rs667066	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs673938	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs674770	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs683010	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs684022	0.81[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834654	chr3:34747802-34916657	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv834655	chr3:34752929-34898824	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3415700	chr3:34806371-34914306	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:34814800-34821800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr3:34818000-34824200	Weak transcription	Aorta	Aorta

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