Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:94603930..94606301-chr5:94606313..94609446,3	K562	blood:

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10059467	0.82[AFR][1000 genomes]
rs27688	0.87[ASN][1000 genomes]
rs397826	0.94[ASN][1000 genomes]
rs421754	0.94[ASN][1000 genomes]
rs443272	0.89[ASN][1000 genomes]
rs448433	0.94[ASN][1000 genomes]
rs455516	0.98[ASN][1000 genomes]
rs457568	0.85[ASN][1000 genomes]
rs457819	0.95[ASN][1000 genomes]
rs458134	0.94[ASN][1000 genomes]
rs458663	0.92[ASN][1000 genomes]
rs458978	0.97[ASN][1000 genomes]
rs459730	0.97[ASN][1000 genomes]
rs460102	0.98[ASN][1000 genomes]
rs460363	0.97[ASN][1000 genomes]
rs460924	0.94[ASN][1000 genomes]
rs461059	0.97[ASN][1000 genomes]
rs462526	0.95[ASN][1000 genomes]
rs462828	0.92[ASN][1000 genomes]
rs462862	0.92[ASN][1000 genomes]
rs463261	0.92[ASN][1000 genomes]
rs463587	0.91[ASN][1000 genomes]
rs463961	0.92[ASN][1000 genomes]
rs464001	0.92[ASN][1000 genomes]
rs464008	0.92[ASN][1000 genomes]
rs464084	0.95[ASN][1000 genomes]
rs464906	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs464971	0.92[ASN][1000 genomes]
rs465847	0.94[ASN][1000 genomes]
rs467144	0.98[ASN][1000 genomes]
rs669335	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[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	nsv432752	chr5:94524244-94691044	Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr5:94602400-94616200	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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