Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:155679304..155682276-chr3:155682932..155686695,3	K562	blood:

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

rs_ID	r²[population]
rs10936022	0.83[ASN][1000 genomes]
rs11712694	0.81[ASN][1000 genomes]
rs12636569	0.82[ASN][1000 genomes]
rs12638792	0.82[ASN][1000 genomes]
rs12638836	0.82[ASN][1000 genomes]
rs1356252	0.82[ASN][1000 genomes]
rs1711084	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1878211	0.82[ASN][1000 genomes]
rs2067877	0.82[ASN][1000 genomes]
rs28438758	0.82[ASN][1000 genomes]
rs3772112	0.85[ASN][1000 genomes]
rs401514	0.81[ASN][1000 genomes]
rs406701	0.81[ASN][1000 genomes]
rs4679757	0.84[ASN][1000 genomes]
rs4679758	0.87[ASN][1000 genomes]
rs4680222	0.87[ASN][1000 genomes]
rs6441022	0.81[ASN][1000 genomes]
rs6766927	0.81[ASN][1000 genomes]
rs6806109	0.81[ASN][1000 genomes]
rs819844	0.89[ASN][1000 genomes]
rs819854	0.83[ASN][1000 genomes]
rs819858	0.93[ASN][1000 genomes]
rs843931	0.89[ASN][1000 genomes]
rs847800	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs965034	0.83[ASN][1000 genomes]
rs9820534	0.82[ASN][1000 genomes]
rs9825321	0.82[ASN][1000 genomes]
rs9846097	0.81[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	nsv877680	chr3:155438022-155723064	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	esv2753744	chr3:155487298-155707298	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:155660400-155688000	Weak transcription	Hela-S3	cervix
2	chr3:155664600-155681200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr3:155674200-155681600	Weak transcription	NH-A	brain
4	chr3:155677800-155681200	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr3:155678000-155680400	Weak transcription	Osteobl	bone
6	chr3:155678000-155681400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr3:155678400-155681400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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