Variant report

Variant	rs4287026
Chromosome Location	chr9:19016306-19016307
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 80 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:74)

rs_ID	r²[population]
rs10116436	0.85[ASN][1000 genomes]
rs10121747	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10125038	0.85[ASN][1000 genomes]
rs10757018	0.89[ASN][1000 genomes]
rs10757021	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10811073	0.81[ASN][1000 genomes]
rs10811074	0.81[ASN][1000 genomes]
rs10811075	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10811076	0.84[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10811078	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10811079	0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10811080	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10811081	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10811082	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10811083	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10811084	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10811085	0.84[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10811099	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10811100	0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10963894	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10963896	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10963897	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10963898	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10963907	0.92[ASN][1000 genomes]
rs10963909	0.86[ASN][1000 genomes]
rs10963910	0.90[ASN][1000 genomes]
rs10963911	0.90[ASN][1000 genomes]
rs10963912	0.86[ASN][1000 genomes]
rs11790123	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs12352657	0.85[ASN][1000 genomes]
rs12352756	0.87[ASN][1000 genomes]
rs12553946	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13284512	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17236081	0.89[ASN][1000 genomes]
rs1932447	0.81[ASN][1000 genomes]
rs1932452	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1932453	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2152463	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2152464	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2383082	0.85[ASN][1000 genomes]
rs2383083	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35150512	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3892045	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4130084	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56254400	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62560430	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6475299	0.82[ASN][1000 genomes]
rs6475300	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs6475305	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6475306	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs66688010	0.91[ASN][1000 genomes]
rs7020294	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7024697	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7025123	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7028858	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7028936	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7029677	0.87[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7037262	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7037837	0.83[ASN][1000 genomes]
rs7038730	0.84[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7048386	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7848929	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7852907	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7857590	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7861842	0.84[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7864376	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7864909	0.85[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs7864930	0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7867428	0.83[ASN][1000 genomes]
rs7870547	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7871030	0.83[ASN][1000 genomes]
rs7871205	0.83[ASN][1000 genomes]
rs7871505	0.83[ASN][1000 genomes]
rs7875035	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv892692	chr9:18519699-19045502	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv1017820	chr9:18882219-19587377	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
3	nsv540078	chr9:18882219-19587377	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
4	nsv892699	chr9:18945868-19025693	Weak transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv892700	chr9:18979441-19156784	Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
6	nsv892701	chr9:18999837-19032907	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:19016200-19021800	Weak transcription	Aorta	Aorta

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