Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:46229589..46231400-chr3:46238254..46240186,2	K562	blood:
2	chr3:46235082..46237927-chr3:46239251..46241191,2	K562	blood:

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs11914967	1.00[TSI][hapmap]
rs11918542	1.00[EUR][1000 genomes]
rs11922302	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11929424	1.00[EUR][1000 genomes]
rs11929453	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs11929460	1.00[EUR][1000 genomes]
rs13062450	0.89[AFR][1000 genomes]
rs13082995	0.86[AFR][1000 genomes]
rs17078685	1.00[EUR][1000 genomes]
rs17078694	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17078698	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3136673	0.89[AFR][1000 genomes]
rs41405546	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41434946	0.80[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41459051	0.81[AFR][1000 genomes]
rs41491548	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41491747	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41511545	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41537245	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56093858	1.00[EUR][1000 genomes]
rs56277808	1.00[EUR][1000 genomes]
rs60714453	1.00[EUR][1000 genomes]
rs73830780	1.00[EUR][1000 genomes]
rs73830781	1.00[EUR][1000 genomes]
rs73830796	1.00[EUR][1000 genomes]
rs7615337	1.00[EUR][1000 genomes]
rs7653045	1.00[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv876734	chr3:45725031-46468467	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv498008	chr3:45733423-46319401	Strong transcription Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46235200-46241800	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr3:46235400-46247600	Weak transcription	Placenta	Placenta
3	chr3:46235400-46249600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr3:46236800-46241200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr3:46237000-46241200	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr3:46237000-46241600	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr3:46239600-46243800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr3:46239800-46249400	Weak transcription	Primary T cells from cord blood	blood

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