Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10746363	0.96[CEU][hapmap];0.96[EUR][1000 genomes]
rs10779265	0.96[CEU][hapmap];0.96[EUR][1000 genomes]
rs11117606	0.97[EUR][1000 genomes]
rs12027943	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs1833037	0.81[CHB][hapmap]
rs2065804	0.96[CEU][hapmap];0.96[EUR][1000 genomes]
rs2376831	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs2784467	0.95[EUR][1000 genomes]
rs2784468	0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2799470	0.97[EUR][1000 genomes]
rs2809293	0.96[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2809294	0.96[CEU][hapmap];0.97[EUR][1000 genomes]
rs2818957	0.97[EUR][1000 genomes]
rs2818959	0.97[EUR][1000 genomes]
rs2818960	0.96[CEU][hapmap];0.97[EUR][1000 genomes]
rs2818961	0.97[EUR][1000 genomes]
rs2818962	0.97[EUR][1000 genomes]
rs2818964	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6604626	0.96[CEU][hapmap];0.96[EUR][1000 genomes]
rs6604627	0.87[CHB][hapmap]
rs6673734	0.96[CEU][hapmap];0.96[EUR][1000 genomes]
rs7514191	0.96[EUR][1000 genomes]
rs945453	0.92[CEU][hapmap];0.94[EUR][1000 genomes]
rs945454	0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv549199	chr1:216384908-216814702	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv1003815	chr1:216504235-216836498	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv535289	chr1:216504235-216836498	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	nsv1011849	chr1:216668381-216701163	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:216672200-216699600	Weak transcription	Gastric	stomach
2	chr1:216673200-216704600	Weak transcription	Pancreas	Pancrea
3	chr1:216674600-216702000	Weak transcription	Fetal Intestine Small	intestine
4	chr1:216680600-216691800	Weak transcription	Placenta	Placenta
5	chr1:216680600-216694000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr1:216680600-216704600	Weak transcription	Left Ventricle	heart

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