Variant report

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs1067969	0.86[ASN][1000 genomes]
rs1068735	0.86[ASN][1000 genomes]
rs12428173	0.86[ASN][1000 genomes]
rs1394318	0.86[ASN][1000 genomes]
rs1606637	0.86[ASN][1000 genomes]
rs17059106	0.86[ASN][1000 genomes]
rs1847506	0.86[ASN][1000 genomes]
rs1849688	0.86[ASN][1000 genomes]
rs186181	0.86[ASN][1000 genomes]
rs186182	0.86[ASN][1000 genomes]
rs1875849	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2655710	0.86[ASN][1000 genomes]
rs2671284	0.86[ASN][1000 genomes]
rs2770917	0.86[ASN][1000 genomes]
rs300324	0.86[ASN][1000 genomes]
rs301634	0.86[ASN][1000 genomes]
rs301686	0.86[ASN][1000 genomes]
rs301693	0.86[ASN][1000 genomes]
rs3119874	1.00[ASN][1000 genomes]
rs3119876	0.86[ASN][1000 genomes]
rs3127055	0.86[ASN][1000 genomes]
rs3850087	0.86[ASN][1000 genomes]
rs3861175	0.86[ASN][1000 genomes]
rs3914416	0.86[ASN][1000 genomes]
rs3914417	0.86[ASN][1000 genomes]
rs4542547	0.86[ASN][1000 genomes]
rs4886278	0.83[ASN][1000 genomes]
rs4886290	0.86[ASN][1000 genomes]
rs7997129	0.86[ASN][1000 genomes]
rs7998134	0.86[ASN][1000 genomes]
rs9563846	0.86[ASN][1000 genomes]
rs9570380	0.86[ASN][1000 genomes]
rs9592083	1.00[AMR][1000 genomes]
rs9598176	0.86[ASN][1000 genomes]
rs9598193	0.86[ASN][1000 genomes]
rs9598199	0.86[ASN][1000 genomes]
rs9598206	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[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	chr13:61489200-61489600	Enhancers	Fetal Brain Male	brain

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