Variant report

Variant	rs9497484
Chromosome Location	chr6:146533723-146533724
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs17075748	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2056995	0.94[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs2056996	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2056997	0.93[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs2206516	0.95[EUR][1000 genomes]
rs2223587	0.86[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs2328729	0.95[EUR][1000 genomes]
rs28368752	0.95[EUR][1000 genomes]
rs28734879	0.95[EUR][1000 genomes]
rs4551188	0.95[ASN][1000 genomes]
rs4895693	0.92[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs4895694	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4896861	0.92[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs4896862	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57501950	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs58938823	0.92[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs59450158	0.95[EUR][1000 genomes]
rs6570740	0.95[EUR][1000 genomes]
rs6570747	0.86[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs6570748	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6570752	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6899461	0.95[EUR][1000 genomes]
rs6900892	0.94[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs6914239	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6941146	0.85[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs7744909	0.87[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs9497500	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9497501	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9497515	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs990519	0.87[AFR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv604839	chr6:146305810-146828922	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv830836	chr6:146423405-146598983	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:146532600-146534400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr6:146533200-146534400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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