Variant report

Variant	rs7869609
Chromosome Location	chr9:15760698-15760699
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 113 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:107)

rs_ID	r²[population]
rs10756687	0.91[YRI][hapmap]
rs10756690	0.92[YRI][hapmap]
rs10810399	0.83[YRI][hapmap]
rs10810401	0.92[YRI][hapmap]
rs10962193	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10962194	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1169470	0.90[JPT][hapmap]
rs1177610	0.90[JPT][hapmap]
rs1177611	0.90[JPT][hapmap]
rs11999303	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs12000772	1.00[CHB][hapmap]
rs12005062	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs12005485	1.00[EUR][1000 genomes]
rs12005521	1.00[EUR][1000 genomes]
rs12682932	1.00[CHB][hapmap];0.82[YRI][hapmap]
rs12683523	0.86[CHB][hapmap]
rs12684785	0.85[CHB][hapmap];0.89[JPT][hapmap]
rs12684808	0.86[CHB][hapmap];0.89[JPT][hapmap]
rs12685963	1.00[EUR][1000 genomes]
rs1328287	0.89[JPT][hapmap]
rs1396705	0.86[CHB][hapmap];0.90[JPT][hapmap];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1533040	0.91[YRI][hapmap]
rs1536685	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs1536686	0.90[JPT][hapmap]
rs1536687	0.90[JPT][hapmap]
rs1578558	1.00[CHB][hapmap]
rs16933504	0.90[JPT][hapmap];1.00[EUR][1000 genomes]
rs16933544	0.85[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16933593	0.83[YRI][hapmap];0.86[AFR][1000 genomes]
rs16933603	0.83[YRI][hapmap];0.85[AFR][1000 genomes]
rs16933626	0.89[YRI][hapmap];0.85[AFR][1000 genomes]
rs16933805	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs16933814	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs1815697	0.90[JPT][hapmap]
rs1935220	0.89[JPT][hapmap]
rs1935221	0.89[JPT][hapmap]
rs2066291	1.00[CHB][hapmap];0.83[YRI][hapmap];0.84[AFR][1000 genomes]
rs2094519	0.89[JPT][hapmap]
rs2105314	0.90[JPT][hapmap]
rs2175082	0.91[YRI][hapmap]
rs2794624	0.90[JPT][hapmap]
rs2794625	0.89[JPT][hapmap]
rs2794627	0.89[JPT][hapmap]
rs2794628	0.90[JPT][hapmap]
rs2794632	0.90[JPT][hapmap]
rs2794633	0.89[JPT][hapmap]
rs2987060	0.89[JPT][hapmap]
rs2987061	0.90[JPT][hapmap]
rs2987062	0.89[JPT][hapmap]
rs3008691	0.90[JPT][hapmap]
rs3008693	0.90[JPT][hapmap]
rs3008698	0.90[JPT][hapmap]
rs34816651	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4372097	0.86[CHB][hapmap]
rs4740615	0.91[YRI][hapmap]
rs59761231	0.89[ASN][1000 genomes]
rs60572069	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6474950	0.85[JPT][hapmap];0.86[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs6474968	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7021778	0.90[JPT][hapmap];0.92[YRI][hapmap]
rs7022810	0.93[ASN][1000 genomes]
rs7025415	0.83[YRI][hapmap];0.84[AFR][1000 genomes]
rs7026090	1.00[CHB][hapmap];0.86[JPT][hapmap];1.00[EUR][1000 genomes]
rs7026629	0.84[AFR][1000 genomes]
rs7029375	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs7029410	1.00[CHB][hapmap];0.86[JPT][hapmap];1.00[EUR][1000 genomes]
rs7032595	0.85[CHB][hapmap];0.89[JPT][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7035048	0.86[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7036674	0.91[YRI][hapmap]
rs7039881	1.00[CHB][hapmap]
rs7040071	1.00[CHB][hapmap];0.88[JPT][hapmap];1.00[EUR][1000 genomes]
rs7040549	1.00[EUR][1000 genomes]
rs7040580	1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[EUR][1000 genomes]
rs7044984	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs7048479	0.88[CHB][hapmap];0.84[AFR][1000 genomes]
rs73416209	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73416213	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73416233	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73416254	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73416261	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73416267	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73416285	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73418137	0.85[AFR][1000 genomes]
rs7388793	1.00[CHB][hapmap]
rs770194	1.00[CHB][hapmap]
rs770198	1.00[CHB][hapmap]
rs770199	1.00[CHB][hapmap]
rs770200	1.00[CHB][hapmap]
rs770201	1.00[CHB][hapmap]
rs770202	1.00[CHB][hapmap]
rs770207	0.90[JPT][hapmap]
rs770219	0.89[JPT][hapmap]
rs7847946	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7852250	1.00[CHB][hapmap]
rs7854094	1.00[ASN][1000 genomes]
rs7856304	0.81[AFR][1000 genomes]
rs7861533	1.00[EUR][1000 genomes]
rs7865705	0.83[YRI][hapmap];0.85[AFR][1000 genomes]
rs7866472	0.86[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap]
rs7866699	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];1.00[EUR][1000 genomes]
rs7867018	1.00[CHB][hapmap];0.89[JPT][hapmap];0.82[YRI][hapmap];1.00[EUR][1000 genomes]
rs7867521	0.82[AFR][1000 genomes]
rs7870166	1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7870244	1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7873842	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7874533	0.82[YRI][hapmap]
rs906798	0.90[AFR][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	nsv892625	chr9:15326251-16064850	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv892627	chr9:15397969-15909450	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	esv2752286	chr9:15578017-15794897	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv892632	chr9:15590116-15869845	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv892633	chr9:15604746-15889411	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv892635	chr9:15731775-15876507	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15742600-15769600	Weak transcription	Psoas Muscle	Psoas
2	chr9:15756200-15790800	Weak transcription	Primary hematopoietic stem cells	blood
3	chr9:15757800-15763200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr9:15759200-15784400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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