Variant report

Variant	rs35141318
Chromosome Location	chr10:44602002-44602003
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs10218996	0.83[AFR][1000 genomes]
rs10508882	0.81[AFR][1000 genomes]
rs10899980	0.88[AMR][1000 genomes]
rs10899985	0.93[AFR][1000 genomes]
rs11238853	0.81[AFR][1000 genomes]
rs11238857	0.87[AFR][1000 genomes]
rs11238858	0.82[AFR][1000 genomes]
rs11238867	0.83[AFR][1000 genomes]
rs11238869	0.83[AFR][1000 genomes]
rs11238870	0.83[AFR][1000 genomes]
rs11238873	0.83[AFR][1000 genomes]
rs11814490	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11815950	0.83[AFR][1000 genomes]
rs11817296	0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12254583	0.93[AFR][1000 genomes]
rs12254704	0.91[AFR][1000 genomes]
rs12258788	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12263005	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12265136	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12265471	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12265921	0.83[AFR][1000 genomes]
rs12266428	0.83[AFR][1000 genomes]
rs12267582	0.86[AFR][1000 genomes]
rs12268501	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12763847	0.82[AFR][1000 genomes]
rs12764460	0.83[AFR][1000 genomes]
rs12766445	0.83[AFR][1000 genomes]
rs12774482	0.92[AFR][1000 genomes]
rs12775481	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs17155030	0.83[ASN][1000 genomes]
rs17155150	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1873758	0.83[AFR][1000 genomes]
rs34012822	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35178639	0.81[AFR][1000 genomes]
rs35224046	0.86[AFR][1000 genomes]
rs35874476	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4948602	0.83[AFR][1000 genomes]
rs4948607	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4948824	0.88[AFR][1000 genomes]
rs4948830	0.91[AFR][1000 genomes]
rs4948831	0.95[ASN][1000 genomes]
rs4948834	0.98[ASN][1000 genomes]
rs4948835	0.93[AFR][1000 genomes]
rs4948836	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4948837	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4948839	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4948840	0.83[AFR][1000 genomes]
rs4948845	0.83[AFR][1000 genomes]
rs4948846	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs55774075	0.86[AFR][1000 genomes]
rs58626048	0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59750388	0.98[ASN][1000 genomes]
rs6593400	0.83[AFR][1000 genomes]
rs67594964	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7082703	0.81[AFR][1000 genomes]
rs7088907	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs71491028	0.86[AFR][1000 genomes]
rs72784830	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72784831	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72784832	0.88[AFR][1000 genomes]
rs72786818	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7901170	0.96[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs7901445	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7904643	0.83[AFR][1000 genomes]
rs7909907	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7913521	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[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	chr10:44601200-44603000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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