Variant report

Variant	rs9815232
Chromosome Location	chr3:86678479-86678480
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs1158572	0.89[EUR][1000 genomes]
rs12631630	0.87[EUR][1000 genomes]
rs12636089	0.89[EUR][1000 genomes]
rs12637404	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13068976	0.90[EUR][1000 genomes]
rs13089444	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs35026018	0.89[EUR][1000 genomes]
rs35725686	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4331677	0.89[EUR][1000 genomes]
rs4423767	0.89[EUR][1000 genomes]
rs4528946	0.91[EUR][1000 genomes]
rs4552353	0.91[EUR][1000 genomes]
rs4555522	0.87[EUR][1000 genomes]
rs4589938	0.90[EUR][1000 genomes]
rs4613455	0.88[EUR][1000 genomes]
rs4634118	0.89[EUR][1000 genomes]
rs4855155	0.91[EUR][1000 genomes]
rs4855157	0.88[EUR][1000 genomes]
rs4855159	0.89[EUR][1000 genomes]
rs60037607	0.88[EUR][1000 genomes]
rs6763447	0.89[EUR][1000 genomes]
rs6797231	0.86[EUR][1000 genomes]
rs6800896	0.88[EUR][1000 genomes]
rs6804348	0.87[EUR][1000 genomes]
rs7621447	0.90[EUR][1000 genomes]
rs7652288	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7652534	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9810220	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9810791	0.81[AFR][1000 genomes]
rs9811859	0.89[EUR][1000 genomes]
rs9822222	0.88[EUR][1000 genomes]
rs9828696	0.86[EUR][1000 genomes]
rs9839138	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9839595	0.89[EUR][1000 genomes]
rs9849115	0.89[EUR][1000 genomes]
rs9854920	0.89[EUR][1000 genomes]
rs9859549	0.89[EUR][1000 genomes]
rs9868939	0.89[EUR][1000 genomes]
rs9869426	0.89[EUR][1000 genomes]
rs9870117	0.91[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877116	chr3:86518318-86964922	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	esv1829775	chr3:86534927-86822085	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	esv3351197	chr3:86661311-86684370	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	n/a
4	nsv877117	chr3:86665408-86927574	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv1009339	chr3:86673173-86725713	Weak transcription Enhancers ZNF genes & repeats Active TSS	lncRNA	2 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:86677600-86682200	Weak transcription	Cortex derived primary cultured neurospheres	brain

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