Variant report

Variant	rs10877089
Chromosome Location	chr12:58676731-58676732
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs10877085	0.95[EUR][1000 genomes]
rs10877086	0.96[EUR][1000 genomes]
rs10877087	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10877088	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10877090	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11172511	0.95[EUR][1000 genomes]
rs11172512	0.95[EUR][1000 genomes]
rs11172513	0.95[EUR][1000 genomes]
rs11172514	0.95[EUR][1000 genomes]
rs11172515	0.95[EUR][1000 genomes]
rs11172516	0.93[EUR][1000 genomes]
rs11172518	0.96[EUR][1000 genomes]
rs11172519	0.96[EUR][1000 genomes]
rs11172520	0.96[EUR][1000 genomes]
rs11172521	0.96[EUR][1000 genomes]
rs11172522	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11834960	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12298303	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12300241	0.93[EUR][1000 genomes]
rs12300281	0.95[EUR][1000 genomes]
rs12301627	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12302422	0.95[EUR][1000 genomes]
rs12302505	0.93[EUR][1000 genomes]
rs12307804	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes]
rs12308636	0.95[EUR][1000 genomes]
rs12308645	0.95[EUR][1000 genomes]
rs12308703	0.95[EUR][1000 genomes]
rs12309499	0.95[EUR][1000 genomes]
rs12312992	0.95[EUR][1000 genomes]
rs12315044	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12316990	0.95[EUR][1000 genomes]
rs12318054	0.93[EUR][1000 genomes]
rs12318525	0.95[EUR][1000 genomes]
rs12318566	0.93[EUR][1000 genomes]
rs12423403	0.95[EUR][1000 genomes]
rs12423429	0.87[EUR][1000 genomes]
rs12423693	0.95[EUR][1000 genomes]
rs12424213	0.95[EUR][1000 genomes]
rs1553380	0.92[EUR][1000 genomes]
rs17502933	0.95[EUR][1000 genomes]
rs17581313	0.95[EUR][1000 genomes]
rs17581466	0.95[EUR][1000 genomes]
rs1847207	0.95[EUR][1000 genomes]
rs1847208	0.95[EUR][1000 genomes]
rs1847209	0.95[EUR][1000 genomes]
rs1881651	0.95[EUR][1000 genomes]
rs1881652	0.95[EUR][1000 genomes]
rs1881653	0.95[EUR][1000 genomes]
rs1881654	0.95[EUR][1000 genomes]
rs1881656	0.95[EUR][1000 genomes]
rs28481485	0.96[EUR][1000 genomes]
rs4760194	0.95[EUR][1000 genomes]
rs4760195	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4760196	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4760376	0.95[EUR][1000 genomes]
rs4760379	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4760380	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61921164	0.94[EUR][1000 genomes]
rs61921165	0.95[EUR][1000 genomes]
rs61921166	0.96[EUR][1000 genomes]
rs61921170	0.96[EUR][1000 genomes]
rs61921171	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61938469	0.93[EUR][1000 genomes]
rs61938470	0.93[EUR][1000 genomes]
rs61938471	0.95[EUR][1000 genomes]
rs61938472	0.95[EUR][1000 genomes]
rs7295858	0.95[EUR][1000 genomes]
rs7300089	0.95[EUR][1000 genomes]
rs73103914	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7315974	0.95[EUR][1000 genomes]
rs7315990	0.95[EUR][1000 genomes]
rs7316690	0.95[EUR][1000 genomes]
rs7980807	0.95[EUR][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	nsv899124	chr12:58391839-58883507	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 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	chr12:58676600-58676800	Enhancers	Fetal Heart	heart

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