Variant report

No.	Distal block	Cell Line	Cell type
1	chr8:106098062..106099625-chr8:106102482..106104994,2	MCF-7	breast:
2	chr8:106098685..106100875-chr8:106101996..106103590,2	K562	blood:
3	chr8:106094210..106096629-chr8:106098616..106100274,3	K562	blood:
4	chr8:106082822..106084651-chr8:106097372..106099591,2	K562	blood:

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

rs_ID	r²[population]
rs1521777	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2030476	1.00[ASN][1000 genomes]
rs2342483	1.00[ASN][1000 genomes]
rs28424250	1.00[ASN][1000 genomes]
rs285778	1.00[ASN][1000 genomes]
rs285784	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs285797	0.87[EUR][1000 genomes]
rs285800	1.00[ASN][1000 genomes]
rs285808	1.00[ASN][1000 genomes]
rs285817	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs285818	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs285821	0.92[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs285831	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs285832	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs285844	0.85[AMR][1000 genomes]
rs285875	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28700873	1.00[ASN][1000 genomes]
rs364605	1.00[ASN][1000 genomes]
rs367858	1.00[ASN][1000 genomes]
rs398324	1.00[ASN][1000 genomes]
rs72676195	1.00[ASN][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	esv2762763	chr8:105943295-106218634	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv891253	chr8:105994885-106251476	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv891254	chr8:106060970-106175867	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:106092600-106102400	Weak transcription	K562	blood

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