Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:16868650..16871366-chr6:16871542..16874154,2	K562	blood:
2	chr6:16871325..16873690-chr6:16876965..16879367,2	MCF-7	breast:

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

rs_ID	r²[population]
rs10214621	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10214623	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10214624	1.00[AMR][1000 genomes]
rs10214782	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1240832	1.00[EUR][1000 genomes]
rs1240836	1.00[EUR][1000 genomes]
rs1240837	1.00[EUR][1000 genomes]
rs1240838	1.00[EUR][1000 genomes]
rs1240840	1.00[EUR][1000 genomes]
rs1776473	1.00[EUR][1000 genomes]
rs2759210	1.00[EUR][1000 genomes]
rs2797806	1.00[EUR][1000 genomes]
rs41390248	1.00[EUR][1000 genomes]
rs6934167	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73725249	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73725253	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73725267	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9464946	0.82[AFR][1000 genomes]
rs9464947	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9464949	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9464954	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9477231	1.00[AMR][1000 genomes]
rs9477236	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1838885	chr6:16866948-16885765	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv1837694	chr6:16866948-16885869	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv1842967	chr6:16866948-16885869	Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Weak transcription	Chromatin interactive region lncRNA	1 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	chr6:16871200-16873000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr6:16872200-16873200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr6:16872600-16874000	Enhancers	Primary hematopoietic stem cells	blood
4	chr6:16872800-16873600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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