Variant report

Variant	rs1352694
Chromosome Location	chr4:158594412-158594413
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11100119	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11100121	0.89[ASN][1000 genomes]
rs11734795	0.83[ASN][1000 genomes]
rs11934695	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11942329	0.82[ASN][1000 genomes]
rs12502036	0.88[ASN][1000 genomes]
rs12648940	0.89[ASN][1000 genomes]
rs13103702	0.89[ASN][1000 genomes]
rs1473501	0.95[ASN][1000 genomes]
rs1490531	0.89[ASN][1000 genomes]
rs1844644	0.95[ASN][1000 genomes]
rs2172016	0.95[ASN][1000 genomes]
rs4484348	0.93[ASN][1000 genomes]
rs4512050	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4691429	0.86[ASN][1000 genomes]
rs4691430	0.88[ASN][1000 genomes]
rs6834140	0.83[EUR][1000 genomes]
rs6836134	0.83[EUR][1000 genomes]
rs6837644	0.84[EUR][1000 genomes]
rs6839727	0.94[ASN][1000 genomes]
rs73857685	0.82[EUR][1000 genomes]
rs73857689	0.86[EUR][1000 genomes]
rs7655036	0.95[ASN][1000 genomes]
rs9307971	1.00[ASN][1000 genomes]
rs964774	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1020294	chr4:157722712-158691771	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv537313	chr4:157722712-158691771	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv1018387	chr4:157959931-158764190	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
4	nsv437448	chr4:158550319-158597491	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv993476	chr4:158550643-159202015	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
6	nsv1026954	chr4:158551136-158594600	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv1022827	chr4:158581163-158594600	Weak transcription Enhancers	Chromatin interactive region	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	chr4:158592200-158595000	Weak transcription	Cortex derived primary cultured neurospheres	brain

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