Variant report

Variant	rs4311651
Chromosome Location	chr8:52654831-52654832
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10088109	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10101657	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10112473	0.84[EUR][1000 genomes]
rs10113743	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10448019	0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11778164	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12541234	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12549383	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12676244	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12678094	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13252521	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13259819	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13261717	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13439031	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2976204	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34067888	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs34773755	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34910552	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35326600	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35363824	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs35423247	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4377955	0.82[EUR][1000 genomes]
rs4382468	0.84[EUR][1000 genomes]
rs4407875	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4421347	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4425745	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4541902	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4554456	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4621801	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4626584	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4873200	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4873570	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4873571	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4873576	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4873592	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs5000332	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6473637	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6473638	0.82[EUR][1000 genomes]
rs6987982	0.82[EUR][1000 genomes]
rs6988401	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7001968	0.81[ASN][1000 genomes]
rs7012655	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7014372	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7018227	0.82[EUR][1000 genomes]
rs71512159	0.89[AFR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7459977	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7830013	0.86[EUR][1000 genomes]
rs8180923	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9284000	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932026	chr8:51858658-52758574	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv817615	chr8:52252405-53023384	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv1018429	chr8:52411443-52878946	Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv1034856	chr8:52411443-52886765	Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv890898	chr8:52579964-52680933	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	esv1817480	chr8:52643151-52654831	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:52644000-52665400	Weak transcription	Right Ventricle	heart

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