Variant report

Variant	rs73268455
Chromosome Location	chr8:69468659-69468660
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs11984913	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11987961	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11988777	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11992043	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11992254	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1347382	0.93[ASN][1000 genomes]
rs1434920	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1434940	0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16934696	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16934717	0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1836519	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2117492	0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2289831	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2289832	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2380473	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2380475	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2380476	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2380477	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2890431	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4455810	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4559226	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4559227	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4576413	0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4995316	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55686711	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55880104	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56042829	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56093828	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56765555	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs57010866	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs59050152	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59121536	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59212785	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs60521673	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs60643160	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs60940064	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6472406	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6472407	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6983285	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6984964	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6989036	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6989387	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6989643	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7000982	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7003926	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7004410	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7009978	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7010609	0.97[ASN][1000 genomes]
rs73266585	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73268457	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73268472	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73268481	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73268487	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73683561	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7814002	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7826286	1.00[ASN][1000 genomes]
rs7826288	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs892705	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9692797	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9692812	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9693077	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9693078	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9694215	1.00[EUR][1000 genomes];1.00[ASN][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	nsv948687	chr8:69041121-69642540	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv890981	chr8:69413110-69534542	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv890982	chr8:69420911-69468914	Bivalent/Poised TSS Enhancers Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	esv3365390	chr8:69442447-69470709	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv1023815	chr8:69442474-69486856	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv890983	chr8:69447339-69503062	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:69467800-69468800	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr8:69467800-69468800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr8:69467800-69477400	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr8:69468400-69478600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr8:69468600-69469000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr8:69468600-69469000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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