Variant report

Variant	rs35228298
Chromosome Location	chr3:85392882-85392883
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1005690	0.90[ASN][1000 genomes]
rs12491352	0.90[ASN][1000 genomes]
rs12497411	0.97[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs1985715	0.90[ASN][1000 genomes]
rs57202752	0.89[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs58416672	0.97[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs60117233	0.92[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs60794345	0.86[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs61288113	0.86[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs61318951	0.97[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs72903204	0.92[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs72903206	0.92[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs72903210	0.92[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs72903211	0.92[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs72903214	0.95[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs72903217	0.89[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs72903224	0.89[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs72903248	0.97[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs72903250	0.97[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs72903253	0.97[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs72903254	0.97[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs72903258	0.97[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs72903261	0.97[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs72903264	0.97[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs72903271	0.97[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs72903274	0.97[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs72921320	0.90[ASN][1000 genomes]
rs72921324	0.90[ASN][1000 genomes]
rs72921330	0.90[ASN][1000 genomes]
rs72921331	0.90[ASN][1000 genomes]
rs72921337	0.90[ASN][1000 genomes]
rs72921344	0.90[ASN][1000 genomes]
rs72921353	0.90[ASN][1000 genomes]
rs72921358	0.90[ASN][1000 genomes]
rs72921359	0.90[ASN][1000 genomes]
rs72921360	0.90[ASN][1000 genomes]
rs72921361	0.90[ASN][1000 genomes]
rs72921365	0.90[ASN][1000 genomes]
rs72921368	0.90[ASN][1000 genomes]
rs72921370	0.84[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs7616336	0.90[ASN][1000 genomes]
rs9830359	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3419993	chr3:85030343-85663403	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
2	esv2753915	chr3:85071410-85624810	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1012601	chr3:85246185-85426996	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv536618	chr3:85246185-85426996	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv948806	chr3:85304744-85463443	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1013407	chr3:85307022-85460325	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
7	nsv870153	chr3:85326695-85426936	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv1002238	chr3:85357855-85719373	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
9	nsv536619	chr3:85357855-85719373	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	1 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	chr3:85391800-85393000	Enhancers	Brain Hippocampus Middle	brain
2	chr3:85391800-85393200	Enhancers	Brain Substantia Nigra	brain
3	chr3:85392400-85393000	Enhancers	Brain Anterior Caudate	brain

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