Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr21:16204438..16207040-chr21:16208422..16210550,2	K562	blood:
2	chr21:16199164..16202875-chr21:16203134..16206995,5	K562	blood:

Variant related genes	Relation type
ENSG00000226406	Chromatin interaction

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

rs_ID	r²[population]
rs10482860	0.85[CEU][hapmap]
rs11909551	0.92[CEU][hapmap]
rs12053660	0.90[CEU][hapmap];0.81[EUR][1000 genomes]
rs13046559	0.81[EUR][1000 genomes]
rs13047199	0.85[CEU][hapmap]
rs13048782	0.91[CEU][hapmap]
rs13048847	0.92[CEU][hapmap]
rs13049498	0.84[EUR][1000 genomes]
rs13052074	0.92[CEU][hapmap]
rs2011512	0.91[CEU][hapmap]
rs2103467	0.92[CEU][hapmap]
rs2822923	0.92[CEU][hapmap];0.85[EUR][1000 genomes]
rs2822924	0.85[CEU][hapmap];0.81[EUR][1000 genomes]
rs2822925	0.84[EUR][1000 genomes]
rs2822927	0.92[CEU][hapmap]
rs2822928	0.81[EUR][1000 genomes]
rs2822929	0.92[CEU][hapmap]
rs2822943	0.80[CEU][hapmap]
rs2822948	0.85[CEU][hapmap]
rs2822949	0.85[CEU][hapmap]
rs2822950	0.83[CEU][hapmap]
rs2822951	0.84[CEU][hapmap]
rs2822956	0.85[CEU][hapmap]
rs2822958	0.89[YRI][hapmap]
rs35076443	0.84[EUR][1000 genomes]
rs4817379	0.92[CEU][hapmap]
rs7277621	1.00[CEU][hapmap];0.81[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs7277958	0.92[CEU][hapmap];0.81[EUR][1000 genomes]
rs7281621	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs8132509	0.92[CEU][hapmap]

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	nsv869911	chr21:16184645-16210579	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:16199200-16204600	Weak transcription	K562	blood

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