Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:73966739..73969723-chr15:73971593..73974165,2	K562	blood:

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

rs_ID	r²[population]
rs11072429	0.84[AFR][1000 genomes]
rs11072430	0.92[CEU][hapmap];0.82[CHB][hapmap];0.92[MEX][hapmap];0.82[TSI][hapmap];0.86[EUR][1000 genomes]
rs11072431	0.83[CEU][hapmap];0.82[CHB][hapmap]
rs11634399	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11637091	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11637315	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12591473	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12594175	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1383616	0.83[MEX][hapmap]
rs2127015	0.87[CEU][hapmap];0.83[CHB][hapmap];0.81[JPT][hapmap];0.81[ASN][1000 genomes]
rs2291013	0.87[CEU][hapmap]
rs4075802	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs56262972	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs56413315	0.80[AMR][1000 genomes]
rs57771618	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57909886	0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs6495075	0.82[CHB][hapmap];0.88[MEX][hapmap];0.80[TSI][hapmap];0.83[EUR][1000 genomes]
rs6495076	0.90[CEU][hapmap];0.85[EUR][1000 genomes]
rs7176654	0.92[CEU][hapmap];0.83[CHB][hapmap];0.86[CHD][hapmap];0.84[GIH][hapmap];0.86[JPT][hapmap];0.96[MEX][hapmap];0.87[TSI][hapmap];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs8023823	0.94[YRI][hapmap]
rs8036954	0.92[CEU][hapmap];0.82[CHB][hapmap];0.87[GIH][hapmap];0.92[MEX][hapmap];0.87[TSI][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9920359	0.83[CEU][hapmap]

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	nsv1037540	chr15:73712637-73982420	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7497012	PML	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:73967400-73969800	Weak transcription	Right Atrium	heart

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