Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10879332	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10879333	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11178706	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1348227	0.88[ASN][1000 genomes]
rs1985044	0.84[AFR][1000 genomes]
rs2405508	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2405511	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2772460	0.97[ASN][1000 genomes]
rs312267	0.93[ASN][1000 genomes]
rs312268	0.94[ASN][1000 genomes]
rs312275	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs312277	0.93[ASN][1000 genomes]
rs312278	0.92[ASN][1000 genomes]
rs312279	0.93[ASN][1000 genomes]
rs312280	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs312281	0.93[ASN][1000 genomes]
rs312284	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4453315	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4767992	0.84[ASN][1000 genomes]
rs61913941	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7968835	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7970381	0.85[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	nsv427909	chr12:41054306-41322257	Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv832380	chr12:41132306-41323961	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:41226800-41266400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:41232000-41248000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

Quick Search: