Variant report

Variant	rs9372551
Chromosome Location	chr6:120092896-120092897
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs1156148	0.89[EUR][1000 genomes]
rs1156149	0.83[EUR][1000 genomes]
rs12197190	0.86[EUR][1000 genomes]
rs1417842	0.86[EUR][1000 genomes]
rs1417844	0.88[EUR][1000 genomes]
rs1417845	0.88[EUR][1000 genomes]
rs1884254	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1964836	0.83[EUR][1000 genomes]
rs2103845	0.87[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs2207611	0.96[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.89[EUR][1000 genomes]
rs2357678	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4310086	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4946435	0.87[EUR][1000 genomes]
rs6569085	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6569089	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6899335	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs767398	0.85[EUR][1000 genomes]
rs7739078	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7763039	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9320700	0.83[EUR][1000 genomes]
rs9372550	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9372553	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9374815	0.87[EUR][1000 genomes]
rs9374819	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9374827	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9387673	0.83[EUR][1000 genomes]
rs9387675	0.95[CEU][hapmap];0.90[CHB][hapmap];0.90[JPT][hapmap];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9387681	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9398521	0.87[EUR][1000 genomes]
rs9401163	0.87[EUR][1000 genomes]
rs9401164	0.82[EUR][1000 genomes]
rs9401171	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9481954	0.86[EUR][1000 genomes]
rs9481958	0.86[CHB][hapmap];0.83[EUR][1000 genomes]
rs9489766	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3447598	chr6:119558591-120119384	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	esv3389526	chr6:119558598-120190087	ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv1028580	chr6:120032073-120095538	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 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	chr6:120092000-120093000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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