Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:120778884..120780620-chr4:120800683..120802958,2	K562	blood:

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10013306	0.95[EUR][1000 genomes]
rs10452196	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10518339	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16997607	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17006835	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17006879	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17006974	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4586911	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs58946926	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6836195	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6845298	0.95[EUR][1000 genomes]
rs6852136	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6855466	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72910441	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72910468	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72910474	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72910481	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72910490	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72910492	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9307481	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9993750	0.95[EUR][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	nsv532739	chr4:120392824-121098103	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120758600-120794000	Weak transcription	Aorta	Aorta
2	chr4:120778000-120780200	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr4:120779200-120780000	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr4:120779400-120780200	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr4:120779600-120780800	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr4:120779600-120781000	Enhancers	ES-I3 Cell Line	embryonic stem cell

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