Variant report

Variant	rs792227
Chromosome Location	chr10:90110108-90110109
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10887807	0.81[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs11202703	0.82[ASN][1000 genomes]
rs11202705	0.84[ASN][1000 genomes]
rs11202706	0.83[ASN][1000 genomes]
rs11202722	0.88[ASN][1000 genomes]
rs11202726	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs11202731	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11202734	0.89[ASN][1000 genomes]
rs11528433	0.84[ASN][1000 genomes]
rs11598623	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12217988	0.81[ASN][1000 genomes]
rs12219831	0.84[ASN][1000 genomes]
rs12220632	0.93[ASN][1000 genomes]
rs12221213	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12569922	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12572813	0.84[ASN][1000 genomes]
rs1426617	0.84[ASN][1000 genomes]
rs1582223	0.89[ASN][1000 genomes]
rs1582224	0.81[ASN][1000 genomes]
rs1613409	0.89[ASN][1000 genomes]
rs1648512	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1648523	0.89[ASN][1000 genomes]
rs17111200	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs1774970	0.81[ASN][1000 genomes]
rs1774971	0.89[ASN][1000 genomes]
rs2195013	0.82[ASN][1000 genomes]
rs2241515	0.87[ASN][1000 genomes]
rs3740279	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3781201	0.90[ASN][1000 genomes]
rs55749454	0.90[ASN][1000 genomes]
rs57949777	0.82[ASN][1000 genomes]
rs59184458	0.82[ASN][1000 genomes]
rs59482232	0.82[ASN][1000 genomes]
rs61260851	0.82[ASN][1000 genomes]
rs7075138	0.90[ASN][1000 genomes]
rs74149704	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs74149712	0.82[ASN][1000 genomes]
rs74149714	0.87[ASN][1000 genomes]
rs74149715	0.87[ASN][1000 genomes]
rs752709	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7919335	0.83[ASN][1000 genomes]
rs792224	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs792225	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs792226	0.89[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs792228	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs792229	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs880793	0.87[ASN][1000 genomes]
rs880794	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895879	chr10:90015725-90219298	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv551838	chr10:90058637-90137045	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv482385	chr10:90066140-90259751	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv948664	chr10:90076715-90517150	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 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	chr10:90108200-90112400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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