Variant report

Variant	rs12775481
Chromosome Location	chr10:44605876-44605877
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10899980	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10899985	0.81[AFR][1000 genomes]
rs11814490	0.94[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11817296	0.92[AMR][1000 genomes]
rs12258788	0.94[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12263005	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12265136	0.92[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12265471	0.94[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12268501	0.96[AMR][1000 genomes]
rs17155150	0.94[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs34012822	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs35141318	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs35874476	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4948607	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4948831	0.82[ASN][1000 genomes]
rs4948834	0.82[ASN][1000 genomes]
rs4948836	0.96[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4948837	0.96[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4948839	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4948846	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs58626048	0.92[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs59750388	0.82[ASN][1000 genomes]
rs67594964	0.94[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs7088907	0.86[AMR][1000 genomes]
rs72784830	0.94[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs72784831	0.94[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs72786818	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7901170	0.83[AFR][1000 genomes]
rs7901445	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7909907	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7913521	0.94[AMR][1000 genomes];0.82[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	nsv1038511	chr10:44596885-44870030	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 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	chr10:44603800-44607400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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