Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:177740310..177743198-chr3:177745813..177748789,2	K562	blood:

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs16828884	1.00[ASN][1000 genomes]
rs1895070	1.00[ASN][1000 genomes]
rs2080668	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2863063	1.00[ASN][1000 genomes]
rs4502028	1.00[ASN][1000 genomes]
rs4533667	1.00[ASN][1000 genomes]
rs4579029	1.00[ASN][1000 genomes]
rs56965193	1.00[ASN][1000 genomes]
rs57660332	1.00[ASN][1000 genomes]
rs62283967	1.00[ASN][1000 genomes]
rs62283968	1.00[ASN][1000 genomes]
rs62283969	1.00[ASN][1000 genomes]
rs62283970	1.00[ASN][1000 genomes]
rs62283971	1.00[ASN][1000 genomes]
rs62283972	1.00[ASN][1000 genomes]
rs62283973	1.00[ASN][1000 genomes]
rs62283974	1.00[ASN][1000 genomes]
rs62283975	1.00[ASN][1000 genomes]
rs62283978	1.00[ASN][1000 genomes]
rs62283979	1.00[ASN][1000 genomes]
rs62283981	1.00[ASN][1000 genomes]
rs6763564	1.00[ASN][1000 genomes]
rs6764673	1.00[ASN][1000 genomes]
rs6767647	1.00[ASN][1000 genomes]
rs6788525	1.00[ASN][1000 genomes]
rs6804858	1.00[ASN][1000 genomes]
rs6805270	1.00[ASN][1000 genomes]
rs727335	1.00[ASN][1000 genomes]
rs7430015	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7645340	1.00[ASN][1000 genomes]
rs9290633	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9757291	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9852369	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9861535	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][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	nsv931055	chr3:177229521-177889872	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv829805	chr3:177662113-177805003	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr3:177739800-177742200	Weak transcription	Aorta	Aorta
2	chr3:177740000-177741600	Enhancers	Colon Smooth Muscle	Colon

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