Variant report

Variant	rs13090291
Chromosome Location	chr3:161777076-161777077
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 93 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:89)

rs_ID	r²[population]
rs1119974	0.82[ASN][1000 genomes]
rs1119975	0.99[ASN][1000 genomes]
rs1119976	0.99[ASN][1000 genomes]
rs1119977	0.97[ASN][1000 genomes]
rs11922869	0.85[ASN][1000 genomes]
rs12630366	0.89[ASN][1000 genomes]
rs12631615	0.99[ASN][1000 genomes]
rs12637049	0.99[ASN][1000 genomes]
rs12638307	0.89[ASN][1000 genomes]
rs12638648	0.99[ASN][1000 genomes]
rs12638716	0.99[ASN][1000 genomes]
rs13067265	0.97[ASN][1000 genomes]
rs13067435	0.95[ASN][1000 genomes]
rs13067436	0.97[ASN][1000 genomes]
rs13071617	0.88[ASN][1000 genomes]
rs13080578	0.87[ASN][1000 genomes]
rs13085452	0.99[ASN][1000 genomes]
rs13085482	0.99[ASN][1000 genomes]
rs13086633	0.87[ASN][1000 genomes]
rs13087182	0.86[ASN][1000 genomes]
rs13090130	0.86[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs13097361	0.99[ASN][1000 genomes]
rs13100661	0.92[ASN][1000 genomes]
rs1397236	0.92[ASN][1000 genomes]
rs1397240	0.92[ASN][1000 genomes]
rs1397241	0.92[ASN][1000 genomes]
rs1397242	0.92[ASN][1000 genomes]
rs1397243	0.92[ASN][1000 genomes]
rs1397244	0.92[ASN][1000 genomes]
rs1397245	0.92[ASN][1000 genomes]
rs1510340	0.89[ASN][1000 genomes]
rs16834360	0.92[ASN][1000 genomes]
rs1813301	0.82[ASN][1000 genomes]
rs1912454	0.89[ASN][1000 genomes]
rs2089737	0.82[ASN][1000 genomes]
rs2102508	0.97[ASN][1000 genomes]
rs2102509	0.97[ASN][1000 genomes]
rs28413956	0.89[ASN][1000 genomes]
rs34793869	0.92[ASN][1000 genomes]
rs34869298	0.97[ASN][1000 genomes]
rs34880574	0.99[ASN][1000 genomes]
rs34922593	0.92[ASN][1000 genomes]
rs35282795	0.92[ASN][1000 genomes]
rs35298688	0.97[ASN][1000 genomes]
rs35512559	0.92[ASN][1000 genomes]
rs35648700	0.97[ASN][1000 genomes]
rs35888322	0.97[ASN][1000 genomes]
rs4323020	0.90[ASN][1000 genomes]
rs4450831	0.89[ASN][1000 genomes]
rs4459917	0.85[ASN][1000 genomes]
rs4498059	0.89[ASN][1000 genomes]
rs4498060	0.89[ASN][1000 genomes]
rs4611839	0.97[ASN][1000 genomes]
rs4856665	0.89[ASN][1000 genomes]
rs4856668	0.82[ASN][1000 genomes]
rs4856669	0.97[ASN][1000 genomes]
rs4856744	0.97[ASN][1000 genomes]
rs4856746	0.82[ASN][1000 genomes]
rs4856763	0.85[ASN][1000 genomes]
rs4856765	0.81[ASN][1000 genomes]
rs56210893	0.97[ASN][1000 genomes]
rs56315604	0.90[ASN][1000 genomes]
rs56400336	0.89[ASN][1000 genomes]
rs62278873	0.82[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs62278939	0.97[ASN][1000 genomes]
rs6762210	0.97[ASN][1000 genomes]
rs6776232	0.97[ASN][1000 genomes]
rs6778769	0.81[ASN][1000 genomes]
rs6779000	0.93[ASN][1000 genomes]
rs6779195	0.97[ASN][1000 genomes]
rs6789071	0.92[ASN][1000 genomes]
rs6789187	0.82[ASN][1000 genomes]
rs6789427	0.97[ASN][1000 genomes]
rs6789851	0.82[ASN][1000 genomes]
rs6791872	0.97[ASN][1000 genomes]
rs6796554	0.92[ASN][1000 genomes]
rs6800261	0.99[ASN][1000 genomes]
rs71635264	0.84[ASN][1000 genomes]
rs7432475	0.97[ASN][1000 genomes]
rs7615800	0.97[ASN][1000 genomes]
rs7626556	0.82[ASN][1000 genomes]
rs7637893	0.97[ASN][1000 genomes]
rs907079	0.89[ASN][1000 genomes]
rs907080	0.89[ASN][1000 genomes]
rs951475	0.92[ASN][1000 genomes]
rs9816747	0.82[ASN][1000 genomes]
rs9840976	0.89[ASN][1000 genomes]
rs9876455	0.82[ASN][1000 genomes]
rs993596	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533237	chr3:161019834-161804660	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	91 gene(s)	inside rSNPs	diseases
2	nsv460918	chr3:161754109-161791399	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
3	nsv592143	chr3:161754109-161791399	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
4	nsv979792	chr3:161775568-161780695	ZNF genes & repeats	n/a	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	chr3:161777000-161777600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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