Variant report

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

rs_ID	r²[population]
rs10509003	0.96[CEU][hapmap]
rs10825135	0.82[CEU][hapmap]
rs10825137	0.81[CEU][hapmap]
rs10825165	0.96[CEU][hapmap]
rs11003923	0.89[CEU][hapmap]
rs11003961	0.96[CEU][hapmap]
rs11003972	0.96[CEU][hapmap]
rs11003979	1.00[CEU][hapmap]
rs11003981	1.00[CEU][hapmap]
rs11003984	0.96[CEU][hapmap]
rs11004000	0.93[JPT][hapmap]
rs12763785	1.00[CEU][hapmap]
rs16937872	0.80[JPT][hapmap]
rs17709865	0.96[CEU][hapmap]
rs2135724	1.00[CEU][hapmap];0.89[CHB][hapmap];0.92[JPT][hapmap]
rs2253882	1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[JPT][hapmap];0.92[YRI][hapmap]
rs2610885	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2610890	1.00[CEU][hapmap];0.88[MEX][hapmap];0.85[EUR][1000 genomes]
rs2610895	1.00[CEU][hapmap];0.91[CHB][hapmap];0.89[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.98[TSI][hapmap]
rs2610896	0.95[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs2610898	0.96[CEU][hapmap];0.87[MEX][hapmap]
rs2660148	0.93[JPT][hapmap]
rs2660149	0.93[JPT][hapmap]
rs2660175	0.96[CEU][hapmap];0.87[MEX][hapmap]
rs2926403	1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[JPT][hapmap];0.92[YRI][hapmap]
rs2939929	1.00[CEU][hapmap];0.91[CHB][hapmap];0.89[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.95[TSI][hapmap]

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	nsv949692	chr10:55502542-55893206	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1052939	chr10:55654719-55769239	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv869303	chr10:55714219-55857931	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:55744600-55745400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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