Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:156573384..156575270-chr3:156577093..156579148,2	K562	blood:

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs13317783	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1991618	0.83[AFR][1000 genomes]
rs56231331	1.00[AMR][1000 genomes]
rs57472927	0.86[AFR][1000 genomes]
rs59077786	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61607068	0.83[AFR][1000 genomes]
rs6763606	0.83[AFR][1000 genomes]
rs6766799	1.00[AMR][1000 genomes]
rs6782196	1.00[AMR][1000 genomes]
rs6783136	1.00[AMR][1000 genomes]
rs73875742	1.00[AMR][1000 genomes]
rs73875746	1.00[AMR][1000 genomes]
rs7625660	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9810073	1.00[AMR][1000 genomes]
rs9811311	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9815241	1.00[AMR][1000 genomes]
rs9824348	1.00[AMR][1000 genomes]
rs9825950	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9839563	1.00[AMR][1000 genomes]
rs9855517	0.86[AFR][1000 genomes]
rs9863865	1.00[YRI][hapmap]
rs9866769	0.83[AFR][1000 genomes]
rs9867597	1.00[YRI][hapmap]
rs9870882	1.00[AMR][1000 genomes]
rs9873640	0.83[AFR][1000 genomes]
rs9883215	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][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	nsv428745	chr3:156405054-156577840	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv877685	chr3:156444383-156611676	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
3	nsv829765	chr3:156568263-156718496	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:156577200-156578000	Enhancers	Primary B cells from peripheral blood	blood
2	chr3:156577200-156578400	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr3:156577400-156578000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr3:156577600-156578400	Enhancers	Monocytes-CD14+_RO01746	blood

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