Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:69210547..69212244-chr1:69212778..69215593,2	K562	blood:

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10889787	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10889788	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10889789	0.86[ASN][1000 genomes]
rs1388654	0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1492064	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1844937	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4625320	0.88[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4926378	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6588337	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs6656449	0.86[ASN][1000 genomes]
rs6672452	0.87[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6680906	0.86[ASN][1000 genomes]
rs6694895	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7523563	0.95[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7527747	0.88[AMR][1000 genomes];0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7531243	0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7534385	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs854272	0.96[ASN][1000 genomes]
rs854273	0.96[ASN][1000 genomes]
rs9326085	0.88[AMR][1000 genomes];0.80[EUR][1000 genomes];0.84[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	nsv527722	chr1:69212053-69323222	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:69211800-69214200	Weak transcription	Fetal Brain Male	brain

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