Variant report

Variant	rs9307551
Chromosome Location	chr4:80530671-80530672
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 71 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10004226	0.94[ASN][1000 genomes]
rs10022663	0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1031004	0.99[ASN][1000 genomes]
rs1031005	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11098762	0.94[ASN][1000 genomes]
rs11098764	0.94[ASN][1000 genomes]
rs11098766	0.94[ASN][1000 genomes]
rs11098770	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1115518	0.95[JPT][hapmap]
rs1115519	0.95[JPT][hapmap]
rs11728755	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11736369	0.87[ASN][1000 genomes]
rs11941782	0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12500146	0.94[ASN][1000 genomes]
rs12501981	0.80[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs12507160	0.94[ASN][1000 genomes]
rs12507375	0.94[ASN][1000 genomes]
rs12511646	0.94[ASN][1000 genomes]
rs12643491	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12643976	0.98[ASN][1000 genomes]
rs13104009	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13112067	0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13112577	0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13124357	0.98[ASN][1000 genomes]
rs13127970	0.90[ASN][1000 genomes]
rs13129838	0.84[ASN][1000 genomes]
rs13142610	1.00[ASN][1000 genomes]
rs13144408	0.81[ASN][1000 genomes]
rs13146986	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs1348086	1.00[ASN][1000 genomes]
rs1371989	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1371993	0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1440852	0.94[ASN][1000 genomes]
rs1440853	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1440854	0.94[ASN][1000 genomes]
rs1440864	0.94[ASN][1000 genomes]
rs17003985	1.00[ASN][1000 genomes]
rs1837645	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1837646	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1866835	0.90[EUR][1000 genomes]
rs1975399	0.94[ASN][1000 genomes]
rs2165386	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2165387	0.92[ASN][1000 genomes]
rs2196978	0.91[ASN][1000 genomes]
rs2582681	0.92[EUR][1000 genomes]
rs2709847	0.92[EUR][1000 genomes]
rs2903640	0.99[ASN][1000 genomes]
rs3109166	0.83[EUR][1000 genomes]
rs35487709	1.00[ASN][1000 genomes]
rs35631270	1.00[ASN][1000 genomes]
rs3943669	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4389603	0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4975056	0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4975057	0.92[ASN][1000 genomes]
rs4975089	0.95[JPT][hapmap]
rs4975097	0.99[ASN][1000 genomes]
rs62297619	0.85[EUR][1000 genomes]
rs62297620	0.85[EUR][1000 genomes]
rs6812760	0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6850999	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6852514	0.94[ASN][1000 genomes]
rs7667469	0.94[ASN][1000 genomes]
rs7688923	0.85[EUR][1000 genomes]
rs894054	0.92[EUR][1000 genomes]
rs894055	0.92[EUR][1000 genomes]
rs9307545	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs968176	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879506	chr4:80316417-80604625	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv879507	chr4:80365765-80552199	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv879508	chr4:80398708-80552199	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1002031	chr4:80459528-80759113	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

Variant related diseases (count:1)

Disease	PMID	Source
Refractive error	23396134	GWAS catalog

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs9307551	LINC00989	cis	Muscle Skeletal	GTEx
rs9307551	LINC00989	cis	Whole Blood	GTEx
rs9307551	LINC00989	cis	Skin Sun Exposed Lower leg	GTEx
rs9307551	LINC00989	cis	Adipose Subcutaneous	GTEx

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:80520200-80532600	Weak transcription	Aorta	Aorta
2	chr4:80530600-80532600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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