Variant report

Variant	rs1567837
Chromosome Location	chr8:9680025-9680026
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10098738	0.83[AMR][1000 genomes]
rs10107341	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11249959	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11249960	0.81[ASN][1000 genomes]
rs11249961	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11783922	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12056794	0.86[CHB][hapmap]
rs12114434	0.80[ASN][1000 genomes]
rs12114435	0.80[ASN][1000 genomes]
rs12114977	0.80[ASN][1000 genomes]
rs12548657	0.80[ASN][1000 genomes]
rs12550323	0.80[ASN][1000 genomes]
rs13251619	0.80[ASN][1000 genomes]
rs13260533	0.80[ASN][1000 genomes]
rs17150534	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17150543	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2048653	0.80[ASN][1000 genomes]
rs2048654	0.80[ASN][1000 genomes]
rs2137789	0.83[AMR][1000 genomes]
rs2409618	0.88[GIH][hapmap];0.92[TSI][hapmap]
rs2898223	0.83[AMR][1000 genomes]
rs4840447	0.80[ASN][1000 genomes]
rs4841215	1.00[ASW][hapmap]
rs59902786	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs61060597	0.83[EUR][1000 genomes]
rs6422356	0.86[CHB][hapmap]
rs6980545	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6984624	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6984939	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6985140	0.86[CHB][hapmap]
rs6987405	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6988507	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6990116	0.86[CHB][hapmap]
rs6991395	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7000483	0.81[ASN][1000 genomes]
rs7002962	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7005902	1.00[CEU][hapmap]
rs7006010	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7010154	0.89[ASW][hapmap]
rs7013004	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7018379	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7835778	0.83[AMR][1000 genomes]
rs9644712	0.83[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	nsv530864	chr8:9097498-9914548	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	esv16865	chr8:9642195-9712807	Enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 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	chr8:9679800-9680600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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