Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:114780402..114782926-chr2:114788012..114789725,2	K562	blood:

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10183875	0.94[CEU][hapmap];0.82[CHB][hapmap];0.80[EUR][1000 genomes]
rs10197726	0.85[EUR][1000 genomes]
rs1060906	0.94[CEU][hapmap]
rs156703	0.85[EUR][1000 genomes]
rs156704	0.86[EUR][1000 genomes]
rs156705	0.95[CEU][hapmap];0.82[CHB][hapmap];0.85[EUR][1000 genomes]
rs156709	0.87[EUR][1000 genomes]
rs156710	0.87[EUR][1000 genomes]
rs156711	0.87[EUR][1000 genomes]
rs156712	0.87[EUR][1000 genomes]
rs156714	0.87[EUR][1000 genomes]
rs17269836	0.82[CEU][hapmap]
rs275416	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs276317	0.83[EUR][1000 genomes]
rs276818	0.84[EUR][1000 genomes]
rs276820	0.84[EUR][1000 genomes]
rs276827	1.00[CEU][hapmap];0.82[CHB][hapmap];0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs467954	0.87[EUR][1000 genomes]
rs55701938	0.82[EUR][1000 genomes]
rs55748015	0.82[EUR][1000 genomes]
rs6542187	0.84[EUR][1000 genomes]
rs6705036	0.84[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	nsv874904	chr2:114751691-115605062	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr2:114788800-114789800	Enhancers	Fetal Kidney	kidney

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