Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:60875870..60877485-chr8:60879560..60881950,2	K562	blood:

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs12676407	0.91[EUR][1000 genomes]
rs1497041	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1626773	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16925454	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1955227	0.91[EUR][1000 genomes]
rs4257994	0.81[EUR][1000 genomes]
rs4607595	0.86[EUR][1000 genomes]
rs4738787	0.89[EUR][1000 genomes]
rs475714	0.84[ASN][1000 genomes]
rs488934	0.84[ASN][1000 genomes]
rs493713	0.84[ASN][1000 genomes]
rs527166	0.90[EUR][1000 genomes]
rs56203327	0.81[EUR][1000 genomes]
rs574368	0.82[ASN][1000 genomes]
rs58546633	0.87[EUR][1000 genomes]
rs594035	0.83[ASN][1000 genomes]
rs595330	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs598457	0.84[ASN][1000 genomes]
rs61514252	0.87[EUR][1000 genomes]
rs62510024	0.86[EUR][1000 genomes]
rs627542	0.92[EUR][1000 genomes]
rs6471845	0.89[EUR][1000 genomes]
rs649886	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs668563	0.80[ASN][1000 genomes]
rs671655	0.82[ASN][1000 genomes]
rs674292	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6984918	0.89[EUR][1000 genomes]
rs6985045	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6996720	0.88[EUR][1000 genomes]
rs7001936	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[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	nsv831331	chr8:60770382-60959633	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:60871600-60884800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr8:60879000-60881800	Enhancers	Primary B cells from cord blood	blood
3	chr8:60879600-60882400	Enhancers	Primary B cells from peripheral blood	blood
4	chr8:60880000-60880800	Enhancers	NH-A	brain
5	chr8:60880200-60882200	Enhancers	Dnd41	blood
6	chr8:60880200-60882400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
7	chr8:60880400-60880800	Enhancers	Rectal Smooth Muscle	rectum
8	chr8:60880400-60881000	Enhancers	Brain Substantia Nigra	brain
9	chr8:60880400-60882400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
10	chr8:60880600-60880800	Enhancers	GM12878-XiMat	blood
11	chr8:60880600-60881800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr8:60880600-60882200	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr8:60880600-60882200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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