Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:45441248..45443305-chr11:45447656..45449205,2	K562	blood:

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

rs_ID	r²[population]
rs10160422	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10742753	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10742754	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10742755	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10742756	0.85[EUR][1000 genomes]
rs10769141	0.82[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs1156593	0.85[EUR][1000 genomes]
rs1156594	0.85[EUR][1000 genomes]
rs1387055	0.85[EUR][1000 genomes]
rs1488662	0.82[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs1906582	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1906584	0.85[EUR][1000 genomes]
rs1906585	0.85[EUR][1000 genomes]
rs2044872	0.85[EUR][1000 genomes]
rs2044875	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2167377	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4497379	0.82[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs6485624	0.85[EUR][1000 genomes]
rs7929511	0.85[EUR][1000 genomes]
rs7929683	0.85[EUR][1000 genomes]
rs7942441	0.85[EUR][1000 genomes]
rs7951748	0.85[EUR][1000 genomes]
rs7951947	0.85[EUR][1000 genomes]
rs896345	0.85[EUR][1000 genomes]
rs985140	0.83[EUR][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	nsv530619	chr11:45294176-45553928	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv1045831	chr11:45419113-45580407	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1049520	chr11:45430802-45494235	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
4	nsv541026	chr11:45430802-45494235	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:45436400-45456800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:45444600-45447800	Enhancers	Fetal Brain Male	brain
3	chr11:45445000-45449600	Weak transcription	Spleen	Spleen
4	chr11:45447200-45447800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr11:45447600-45449600	Weak transcription	Aorta	Aorta

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