Variant report

Variant	rs9538990
Chromosome Location	chr13:61539209-61539210
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10454647	0.80[ASN][1000 genomes]
rs11840967	0.95[ASN][1000 genomes]
rs12873856	0.80[ASN][1000 genomes]
rs12874317	0.80[ASN][1000 genomes]
rs1606713	0.80[ASN][1000 genomes]
rs1606714	0.80[ASN][1000 genomes]
rs1857724	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2090140	0.80[ASN][1000 genomes]
rs2134864	0.80[ASN][1000 genomes]
rs2134867	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2203393	0.80[ASN][1000 genomes]
rs2274655	0.95[ASN][1000 genomes]
rs2323085	0.80[ASN][1000 genomes]
rs2671872	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2874956	0.85[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs302885	0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs302887	0.85[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs302892	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs303379	0.82[AMR][1000 genomes]
rs35323626	0.80[ASN][1000 genomes]
rs35381210	0.80[ASN][1000 genomes]
rs3884484	1.00[ASN][1000 genomes]
rs4886288	1.00[CHB][hapmap]
rs71434982	0.80[ASN][1000 genomes]
rs71434984	0.80[ASN][1000 genomes]
rs71434986	0.80[ASN][1000 genomes]
rs73203738	0.80[ASN][1000 genomes]
rs7328316	1.00[ASN][1000 genomes]
rs7981565	0.80[ASN][1000 genomes]
rs7992324	0.80[ASN][1000 genomes]
rs9538992	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9570410	0.81[AFR][1000 genomes]
rs9592078	0.80[ASN][1000 genomes]
rs9592079	0.80[ASN][1000 genomes]
rs9592080	0.80[ASN][1000 genomes]
rs9598207	1.00[ASN][1000 genomes]
rs9598208	0.80[ASN][1000 genomes]
rs9598223	0.80[ASN][1000 genomes]
rs9598225	0.80[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832624	chr13:61383648-61553974	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island lncRNA	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	chr13:61539200-61539400	Enhancers	Fetal Heart	heart

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