Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:159278536..159280740-chr1:159287173..159289621,2	K562	blood:

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs12119226	0.97[AFR][1000 genomes]
rs12119586	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12123454	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12127102	0.92[EUR][1000 genomes]
rs12130400	0.92[EUR][1000 genomes]
rs12131906	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12134212	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12135235	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12143046	0.89[EUR][1000 genomes]
rs16841956	0.92[EUR][1000 genomes]
rs16841988	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16841997	0.97[AFR][1000 genomes]
rs2325931	0.88[AFR][1000 genomes]
rs2325933	0.90[AFR][1000 genomes]
rs3027070	0.80[EUR][1000 genomes]
rs34479145	0.89[EUR][1000 genomes]
rs72711393	0.89[EUR][1000 genomes]
rs72711395	0.89[EUR][1000 genomes]
rs72713608	0.81[AMR][1000 genomes]
rs72713611	0.92[EUR][1000 genomes]
rs72713622	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72713644	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72713647	0.81[AMR][1000 genomes]
rs72713655	0.90[AFR][1000 genomes]
rs72713656	0.90[AFR][1000 genomes]
rs72713657	0.90[AFR][1000 genomes]
rs72713658	0.90[AFR][1000 genomes]
rs72713659	0.86[AFR][1000 genomes]
rs72713662	0.90[AFR][1000 genomes]
rs72713665	0.86[AFR][1000 genomes]
rs72713666	0.86[AFR][1000 genomes]
rs72713670	0.86[AFR][1000 genomes]
rs72713675	0.86[AFR][1000 genomes]
rs74125414	0.89[EUR][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	nsv872487	chr1:159196765-159342439	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv872488	chr1:159218266-159336948	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:159275800-159279200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr1:159278200-159279400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:159278400-159279400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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