Variant report

Variant	rs9830359
Chromosome Location	chr3:85397118-85397119
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs11714549	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12487446	0.84[ASN][1000 genomes]
rs12631345	0.82[ASN][1000 genomes]
rs1368744	0.82[ASN][1000 genomes]
rs1368746	0.84[ASN][1000 genomes]
rs1368747	0.81[AFR][1000 genomes]
rs1433710	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1433712	0.84[ASN][1000 genomes]
rs1433713	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs1465716	0.88[ASN][1000 genomes]
rs1594795	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs1836131	0.82[ASN][1000 genomes]
rs1897698	0.82[ASN][1000 genomes]
rs2018416	0.82[ASN][1000 genomes]
rs2053105	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2163970	0.82[ASN][1000 genomes]
rs35228298	0.81[ASN][1000 genomes]
rs4856270	0.80[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs4856568	0.82[ASN][1000 genomes]
rs6762253	0.82[ASN][1000 genomes]
rs6771447	0.82[ASN][1000 genomes]
rs6772750	0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6809486	0.81[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs7610238	0.82[ASN][1000 genomes]
rs7623369	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs7651113	0.88[ASN][1000 genomes]
rs9309974	0.84[ASN][1000 genomes]
rs9309975	0.81[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs9309978	0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9824386	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs9824840	0.82[ASN][1000 genomes]
rs9833972	0.82[ASN][1000 genomes]
rs9847998	0.84[AFR][1000 genomes]
rs9854888	0.88[ASN][1000 genomes]
rs9866182	0.82[ASN][1000 genomes]
rs9873752	0.81[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs9879417	0.80[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs989534	0.81[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs9990095	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 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
10	nsv1008956	chr3:85394816-85460325	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
11	nsv536620	chr3:85394816-85460325	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
12	nsv1004254	chr3:85394816-85514910	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
13	nsv536621	chr3:85394816-85514910	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
14	esv3418940	chr3:85395812-85398010	Weak transcription ZNF genes & repeats Enhancers	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	chr3:85396800-85397800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain

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