Variant report

Variant	rs7856877
Chromosome Location	chr9:15852445-15852446
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 136 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:123)

rs_ID	r²[population]
rs1081243	0.90[EUR][1000 genomes]
rs1081244	0.86[EUR][1000 genomes]
rs1081245	0.83[AFR][1000 genomes]
rs1081246	0.90[EUR][1000 genomes]
rs1081247	0.90[EUR][1000 genomes]
rs1169469	0.91[EUR][1000 genomes]
rs1169470	0.89[EUR][1000 genomes]
rs1169471	0.87[EUR][1000 genomes]
rs1169472	0.87[EUR][1000 genomes]
rs1169474	0.88[EUR][1000 genomes]
rs1169475	0.84[EUR][1000 genomes]
rs1169476	0.85[EUR][1000 genomes]
rs1169481	0.84[EUR][1000 genomes]
rs1177610	0.89[EUR][1000 genomes]
rs1177611	0.89[EUR][1000 genomes]
rs1184568	0.87[EUR][1000 genomes]
rs1184913	0.84[EUR][1000 genomes]
rs1185652	0.85[EUR][1000 genomes]
rs1186048	0.84[EUR][1000 genomes]
rs12000772	0.91[ASN][1000 genomes]
rs12682932	0.88[ASN][1000 genomes]
rs12683523	0.85[ASN][1000 genomes]
rs12684485	0.80[ASN][1000 genomes]
rs1328281	0.90[EUR][1000 genomes]
rs1341739	0.89[EUR][1000 genomes]
rs1361607	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1361608	0.89[EUR][1000 genomes]
rs1572978	0.82[AFR][1000 genomes]
rs1578556	0.95[EUR][1000 genomes]
rs1578557	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1578558	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1582200	0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1752777	0.87[EUR][1000 genomes]
rs1773046	0.91[EUR][1000 genomes]
rs1773062	0.84[EUR][1000 genomes]
rs1815697	0.90[EUR][1000 genomes]
rs1935220	0.92[EUR][1000 genomes]
rs1935221	0.88[EUR][1000 genomes]
rs1954220	0.90[EUR][1000 genomes]
rs2066291	0.86[ASN][1000 genomes]
rs2066292	0.86[AFR][1000 genomes]
rs2105313	0.88[EUR][1000 genomes]
rs2105314	0.88[EUR][1000 genomes]
rs2149230	0.81[EUR][1000 genomes]
rs2182935	0.81[EUR][1000 genomes]
rs2769714	0.91[EUR][1000 genomes]
rs2769716	0.84[EUR][1000 genomes]
rs2794624	0.88[EUR][1000 genomes]
rs2794625	0.88[EUR][1000 genomes]
rs2794626	0.88[EUR][1000 genomes]
rs2794627	0.88[EUR][1000 genomes]
rs2794628	0.88[EUR][1000 genomes]
rs2794629	0.90[EUR][1000 genomes]
rs2794632	0.91[EUR][1000 genomes]
rs2794633	0.90[EUR][1000 genomes]
rs2987045	0.88[EUR][1000 genomes]
rs2987054	0.80[EUR][1000 genomes]
rs2987057	0.81[EUR][1000 genomes]
rs2987060	0.81[EUR][1000 genomes]
rs2987061	0.81[EUR][1000 genomes]
rs2995024	0.89[EUR][1000 genomes]
rs2995025	0.87[EUR][1000 genomes]
rs3008692	0.81[EUR][1000 genomes]
rs3008693	0.81[EUR][1000 genomes]
rs3008695	0.81[EUR][1000 genomes]
rs57592105	0.88[ASN][1000 genomes]
rs59779354	0.85[ASN][1000 genomes]
rs6474978	0.88[EUR][1000 genomes]
rs6474979	0.90[EUR][1000 genomes]
rs7028328	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7039881	0.98[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7048479	0.81[ASN][1000 genomes]
rs73422714	0.88[ASN][1000 genomes]
rs73422737	0.85[ASN][1000 genomes]
rs7388793	0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs770190	0.90[EUR][1000 genomes]
rs770191	0.81[AFR][1000 genomes]
rs770192	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs770193	0.86[EUR][1000 genomes]
rs770194	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs770195	0.93[EUR][1000 genomes]
rs770197	0.86[EUR][1000 genomes]
rs770198	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs770199	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs770200	0.94[AFR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs770201	0.97[AFR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs770202	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs770203	0.86[EUR][1000 genomes]
rs770204	0.91[EUR][1000 genomes]
rs770205	0.85[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs770206	0.84[EUR][1000 genomes]
rs770207	0.98[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs770210	0.88[EUR][1000 genomes]
rs770212	0.88[EUR][1000 genomes]
rs770214	0.88[EUR][1000 genomes]
rs770217	0.89[EUR][1000 genomes]
rs770218	0.88[EUR][1000 genomes]
rs770219	0.86[EUR][1000 genomes]
rs7852250	0.93[ASN][1000 genomes]
rs7856304	0.85[ASN][1000 genomes]
rs7860354	0.98[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7860463	0.92[EUR][1000 genomes]
rs7860856	0.80[EUR][1000 genomes]
rs7861105	0.81[EUR][1000 genomes]
rs7867521	0.85[ASN][1000 genomes]
rs809493	0.98[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs9298739	0.83[AFR][1000 genomes]
rs9298740	0.83[AFR][1000 genomes]
rs9298741	0.83[AFR][1000 genomes]
rs9406539	0.80[AFR][1000 genomes]
rs9406546	0.92[EUR][1000 genomes]
rs9407651	0.81[AFR][1000 genomes]
rs9407654	0.81[AFR][1000 genomes]
rs9407655	0.81[AFR][1000 genomes]
rs9407656	0.83[AFR][1000 genomes]
rs9407657	0.83[AFR][1000 genomes]
rs9407658	0.83[AFR][1000 genomes]
rs9407662	0.84[AFR][1000 genomes]
rs9407664	0.98[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9407665	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9407668	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9407669	0.83[AFR][1000 genomes]
rs9407671	0.91[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 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	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
4	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
5	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
6	nsv528964	chr9:15760822-15875162	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv892636	chr9:15794858-15876507	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv613666	chr9:15823667-15875162	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv613667	chr9:15823667-15876507	Enhancers ZNF genes & repeats Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv1016226	chr9:15841107-15875321	ZNF genes & repeats Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv1015435	chr9:15841107-15880385	Enhancers ZNF genes & repeats Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv1032081	chr9:15845902-15878115	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	nsv1027790	chr9:15845902-15878841	Enhancers ZNF genes & repeats Active TSS Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15830200-15857200	Weak transcription	Primary hematopoietic stem cells	blood
2	chr9:15845000-15858800	Weak transcription	Thymus	Thymus
3	chr9:15847200-15857600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr9:15849000-15873800	Weak transcription	Fetal Lung	lung
5	chr9:15850000-15852800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr9:15851000-15852600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr9:15851000-15852600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin

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