Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:63254495..63257131-chr17:63257745..63260137,2	K562	blood:

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs12051686	0.88[ASN][1000 genomes]
rs12602631	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1514502	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs16961958	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2109446	0.93[AMR][1000 genomes]
rs2191396	0.90[ASN][1000 genomes]
rs2869590	0.86[ASN][1000 genomes]
rs4790952	0.90[ASN][1000 genomes]
rs4791209	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4791210	0.86[ASN][1000 genomes]
rs56007713	0.80[AMR][1000 genomes]
rs57715929	0.85[AMR][1000 genomes]
rs7217967	0.80[AMR][1000 genomes]
rs72845321	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72845331	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72845338	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs72845356	0.85[AMR][1000 genomes]
rs72845357	0.85[AMR][1000 genomes]
rs740857	0.89[ASN][1000 genomes]
rs8075545	0.82[ASN][1000 genomes]
rs875647	0.86[ASN][1000 genomes]
rs9904971	0.89[ASN][1000 genomes]
rs9915740	0.80[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	nsv530764	chr17:62939944-63278472	Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	nsv482610	chr17:63214370-63372334	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	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	chr17:63253600-63260200	Weak transcription	Pancreas	Pancrea
2	chr17:63255400-63257200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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