Variant report

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs13314950	0.92[YRI][hapmap]
rs17047606	1.00[CEU][hapmap];0.90[TSI][hapmap];0.84[EUR][1000 genomes]
rs17047609	0.90[CEU][hapmap];0.90[TSI][hapmap]
rs17047611	1.00[CEU][hapmap];0.83[GIH][hapmap];0.85[MEX][hapmap];0.90[TSI][hapmap]
rs262226	0.89[CHB][hapmap];0.87[CHD][hapmap]
rs262227	0.89[CHB][hapmap];0.87[CHD][hapmap]
rs262234	0.94[CHB][hapmap];0.84[JPT][hapmap]
rs262236	0.85[ASN][1000 genomes]
rs262237	0.84[CHB][hapmap];0.87[JPT][hapmap];0.85[ASN][1000 genomes]
rs262238	0.84[CHB][hapmap];0.87[CHD][hapmap];0.88[JPT][hapmap];0.85[ASN][1000 genomes]
rs262239	0.85[ASN][1000 genomes]
rs262240	0.85[ASN][1000 genomes]
rs262241	0.84[CHB][hapmap];0.87[CHD][hapmap];0.88[JPT][hapmap];0.87[ASN][1000 genomes]
rs262242	0.84[CHB][hapmap];0.87[JPT][hapmap];0.87[ASN][1000 genomes]
rs262243	0.87[ASN][1000 genomes]
rs262244	0.80[CHB][hapmap];0.86[JPT][hapmap];0.87[ASN][1000 genomes]
rs63108	0.84[CHB][hapmap];0.87[CHD][hapmap];0.88[JPT][hapmap];0.85[ASN][1000 genomes]
rs6769848	0.90[CEU][hapmap];0.83[CHB][hapmap]
rs6774356	0.89[CEU][hapmap];0.89[CHB][hapmap]
rs6776111	0.90[CEU][hapmap]
rs6805785	0.90[CEU][hapmap];0.89[CHB][hapmap];0.81[JPT][hapmap]
rs72626987	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7617495	0.89[CEU][hapmap];0.89[CHB][hapmap]
rs7629408	1.00[CEU][hapmap]
rs7639960	0.89[CEU][hapmap];0.89[CHB][hapmap]
rs957895	0.90[CEU][hapmap];0.89[CHB][hapmap]
rs9879178	1.00[ASW][hapmap]
rs9880049	1.00[ASW][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	esv2752014	chr3:68091879-68416989	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv1010992	chr3:68353191-68388825	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv834721	chr3:68365963-68526394	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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