Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:66499726..66501980-chr17:66744496..66747086,2	K562	blood:

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10468444	0.82[ASN][1000 genomes]
rs10852738	0.85[EUR][1000 genomes]
rs16972996	0.82[ASN][1000 genomes]
rs16973034	0.83[ASN][1000 genomes]
rs2015212	0.83[ASN][1000 genomes]
rs2302235	0.81[ASN][1000 genomes]
rs3785905	0.82[ASN][1000 genomes]
rs55736761	0.82[ASN][1000 genomes]
rs57936225	0.85[EUR][1000 genomes]
rs7221724	0.82[ASN][1000 genomes]
rs72847781	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72847782	0.85[ASN][1000 genomes]
rs72847784	0.83[ASN][1000 genomes]
rs72847785	0.82[ASN][1000 genomes]
rs72847787	0.80[AFR][1000 genomes]
rs72847789	0.82[ASN][1000 genomes]
rs72847794	0.82[ASN][1000 genomes]
rs72847801	0.83[ASN][1000 genomes]
rs74000753	0.81[ASN][1000 genomes]
rs8067357	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8072598	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs8082254	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833523	chr17:66343323-66510461	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	31 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:66494600-66503600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr17:66501600-66502600	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr17:66501600-66503200	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr17:66501800-66502800	Enhancers	Monocytes-CD14+_RO01746	blood

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