Variant report

Variant	rs7901170
Chromosome Location	chr10:44606846-44606847
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10218996	0.85[AFR][1000 genomes]
rs10899985	0.95[AFR][1000 genomes]
rs11238857	0.83[AFR][1000 genomes]
rs11238867	0.85[AFR][1000 genomes]
rs11238869	0.85[AFR][1000 genomes]
rs11238870	0.85[AFR][1000 genomes]
rs11238873	0.85[AFR][1000 genomes]
rs11814490	0.87[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs11815950	0.85[AFR][1000 genomes]
rs11817296	0.84[ASN][1000 genomes]
rs12254583	0.90[AFR][1000 genomes]
rs12254704	0.87[AFR][1000 genomes]
rs12258788	0.91[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs12263005	0.99[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs12265136	0.88[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs12265471	0.91[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs12266428	0.85[AFR][1000 genomes]
rs12267582	0.82[AFR][1000 genomes]
rs12268501	0.92[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs12763847	0.80[AFR][1000 genomes]
rs12774482	0.89[AFR][1000 genomes]
rs12775481	0.83[AFR][1000 genomes]
rs17155150	0.88[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs1873758	0.85[AFR][1000 genomes]
rs34012822	0.91[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs35141318	0.96[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs35178639	0.82[AFR][1000 genomes]
rs35224046	0.82[AFR][1000 genomes]
rs35874476	0.99[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs4948602	0.85[AFR][1000 genomes]
rs4948607	0.99[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs4948824	0.85[AFR][1000 genomes]
rs4948830	0.87[AFR][1000 genomes]
rs4948831	0.91[ASN][1000 genomes]
rs4948834	0.91[ASN][1000 genomes]
rs4948835	0.90[AFR][1000 genomes]
rs4948836	0.93[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs4948837	0.92[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs4948839	0.87[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs4948840	0.85[AFR][1000 genomes]
rs4948845	0.85[AFR][1000 genomes]
rs4948846	0.96[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs55774075	0.82[AFR][1000 genomes]
rs56090994	0.80[AFR][1000 genomes]
rs58626048	0.89[ASN][1000 genomes]
rs59750388	0.91[ASN][1000 genomes]
rs6593400	0.85[AFR][1000 genomes]
rs67594964	0.91[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs7082703	0.83[AFR][1000 genomes]
rs71491028	0.82[AFR][1000 genomes]
rs72784830	0.88[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs72784831	0.88[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs72784832	0.85[AFR][1000 genomes]
rs72786818	0.99[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs7901445	0.99[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs7904643	0.85[AFR][1000 genomes]
rs7909907	0.99[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs7913521	0.82[AFR][1000 genomes];0.91[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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