Variant report

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs11100951	0.83[ASN][1000 genomes]
rs11100955	0.80[ASN][1000 genomes]
rs11100956	0.81[ASN][1000 genomes]
rs11100957	0.81[ASN][1000 genomes]
rs1346596	0.83[ASN][1000 genomes]
rs1346597	0.82[ASN][1000 genomes]
rs1346601	0.81[ASN][1000 genomes]
rs1366693	0.81[ASN][1000 genomes]
rs1429131	0.82[ASN][1000 genomes]
rs1429132	0.81[ASN][1000 genomes]
rs1429135	0.81[ASN][1000 genomes]
rs1429136	0.80[ASN][1000 genomes]
rs1820830	0.83[ASN][1000 genomes]
rs1820831	0.83[ASN][1000 genomes]
rs2082028	0.83[ASN][1000 genomes]
rs2562861	0.81[ASN][1000 genomes]
rs2562862	0.81[ASN][1000 genomes]
rs2562863	0.80[ASN][1000 genomes]
rs2714881	0.81[ASN][1000 genomes]
rs2714882	0.81[ASN][1000 genomes]
rs2714883	0.81[ASN][1000 genomes]
rs2714884	0.81[ASN][1000 genomes]
rs2714897	0.82[ASN][1000 genomes]
rs2953287	0.80[ASN][1000 genomes]
rs4835388	0.82[ASN][1000 genomes]
rs4835393	0.83[ASN][1000 genomes]
rs6537466	0.83[ASN][1000 genomes]
rs6537469	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6537470	0.83[ASN][1000 genomes]
rs6537471	0.83[ASN][1000 genomes]
rs6824518	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6831149	0.81[ASN][1000 genomes]
rs6835652	0.83[ASN][1000 genomes]
rs6841482	0.82[ASN][1000 genomes]
rs6844496	0.83[ASN][1000 genomes]
rs6853240	0.81[ASN][1000 genomes]
rs736551	0.83[ASN][1000 genomes]
rs7698103	0.81[ASN][1000 genomes]
rs9308216	0.82[ASN][1000 genomes]
rs934143	0.81[ASN][1000 genomes]
rs934144	0.81[ASN][1000 genomes]
rs934145	0.83[ASN][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	nsv1024629	chr4:147987351-148277008	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA	3 gene(s)	inside rSNPs	diseases
2	nsv830108	chr4:148114652-148311104	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:148219200-148222600	Weak transcription	Ovary	ovary

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