Variant report

Variant	rs71635264
Chromosome Location	chr3:161766799-161766800
allele	CAGCTA/TGGCTT
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs1119975	0.86[ASN][1000 genomes]
rs1119976	0.86[ASN][1000 genomes]
rs1119977	0.84[ASN][1000 genomes]
rs12630366	0.82[ASN][1000 genomes]
rs12631615	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12637049	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12638307	0.80[ASN][1000 genomes]
rs12638648	0.80[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs12638716	0.80[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs13067265	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs13067435	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs13067436	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs13071617	0.81[ASN][1000 genomes]
rs13085452	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs13085482	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs13090130	0.80[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs13090291	0.84[ASN][1000 genomes]
rs13097361	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs13099598	0.85[AMR][1000 genomes]
rs13100661	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1397236	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1397240	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1397241	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1397242	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1397243	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1397244	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1397245	0.87[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1510340	0.82[ASN][1000 genomes]
rs16834360	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1912454	0.82[ASN][1000 genomes]
rs2102508	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2102509	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs28413956	0.82[ASN][1000 genomes]
rs34793869	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs34869298	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs34880574	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs34922593	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs35282795	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs35298688	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs35512559	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs35648700	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs35888322	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4323020	0.81[ASN][1000 genomes]
rs4450831	0.82[ASN][1000 genomes]
rs4498059	0.82[ASN][1000 genomes]
rs4498060	0.82[ASN][1000 genomes]
rs4611839	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4856665	0.82[ASN][1000 genomes]
rs4856669	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4856744	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs56210893	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs56315604	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs56400336	0.80[ASN][1000 genomes]
rs62278873	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs62278939	0.80[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs6762210	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6776232	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6779000	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs6779195	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6789071	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6789427	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6791872	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6796554	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6800261	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7432475	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7615800	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7637893	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs907079	0.82[ASN][1000 genomes]
rs907080	0.82[ASN][1000 genomes]
rs951475	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9840976	0.82[ASN][1000 genomes]

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	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:161766600-161771000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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