Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:211979527..211981470-chr2:211988454..211991128,2	MCF-7	breast:

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10170004	0.81[ASN][1000 genomes]
rs10497940	0.84[ASN][1000 genomes]
rs12105986	0.96[ASN][1000 genomes]
rs1370619	0.96[ASN][1000 genomes]
rs1370620	0.96[ASN][1000 genomes]
rs1437373	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16824982	0.96[ASN][1000 genomes]
rs4672605	0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs55634207	0.80[ASN][1000 genomes]
rs55997007	0.81[ASN][1000 genomes]
rs56002634	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs56153748	0.94[ASN][1000 genomes]
rs56313456	0.80[ASN][1000 genomes]
rs59214701	0.80[ASN][1000 genomes]
rs59712773	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6723493	0.93[ASN][1000 genomes]
rs6731805	0.94[ASN][1000 genomes]
rs67557079	0.81[ASN][1000 genomes]
rs6760475	0.94[ASN][1000 genomes]
rs67776983	0.96[ASN][1000 genomes]
rs72935675	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72935680	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72937616	0.80[ASN][1000 genomes]
rs72937623	0.81[ASN][1000 genomes]
rs72941619	0.81[ASN][1000 genomes]
rs7564709	0.95[ASN][1000 genomes]
rs9677922	0.80[ASN][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	nsv1012193	chr2:211684524-212072213	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv834521	chr2:211918881-212057872	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv875773	chr2:211973600-212041403	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:211979400-211980600	Enhancers	Muscle Satellite Cultured Cells	--
2	chr2:211979600-211980800	Enhancers	Brain Germinal Matrix	brain
3	chr2:211979800-211980600	Enhancers	Fetal Brain Male	brain
4	chr2:211979800-211981000	Enhancers	HSMM	muscle

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