Variant report

Variant	rs4450760
Chromosome Location	chr3:155941417-155941418
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs1118418	0.84[ASN][1000 genomes]
rs1120745	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11713991	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11915771	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11915832	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11922447	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1353812	0.88[ASN][1000 genomes]
rs1391889	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1391890	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1499051	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs1499052	0.84[ASN][1000 genomes]
rs1499054	0.84[ASN][1000 genomes]
rs1499056	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1546229	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1909372	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1909373	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1909374	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1909375	0.87[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1909376	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2173492	0.82[ASN][1000 genomes]
rs4271877	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4333049	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4355235	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4453801	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4488791	0.84[ASN][1000 genomes]
rs4505650	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4530487	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4577423	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4634068	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4679763	0.80[ASN][1000 genomes]
rs4679764	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4679765	0.82[ASN][1000 genomes]
rs4680249	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6441045	0.80[ASN][1000 genomes]
rs6441046	0.82[ASN][1000 genomes]
rs6441047	0.84[ASN][1000 genomes]
rs6441050	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6441051	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs6775600	0.84[ASN][1000 genomes]
rs6788238	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6806129	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs728382	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7372394	0.84[ASN][1000 genomes]
rs7611194	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7612532	0.80[ASN][1000 genomes]
rs7621586	0.82[ASN][1000 genomes]
rs7633871	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7634800	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7638421	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7640712	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9818040	0.84[ASN][1000 genomes]
rs9857202	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9864967	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9866991	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[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	nsv592085	chr3:155827634-156012679	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1014755	chr3:155889430-156411894	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:155936400-155941600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:155936600-155945400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr3:155936600-155951000	Weak transcription	Aorta	Aorta

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