Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs12819583	0.81[EUR][1000 genomes]
rs1353155	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1389494	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1493819	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1493823	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1493824	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1493825	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2201343	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2605364	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2641489	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2641490	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2641493	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2641495	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2641497	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2641498	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2641500	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2641501	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2661714	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4475988	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs631620	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]

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	nsv1039468	chr12:74080586-75000246	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv899293	chr12:74835107-74995760	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:74990000-74996800	Weak transcription	Stomach Mucosa	stomach
2	chr12:74993400-74994000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr12:74993800-74994400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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