Variant report

Variant	rs1169473
Chromosome Location	chr9:15880752-15880753
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNAPC3-6	chr9:15878981-15880761	ucscGeneNc_uc003zmg_2

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs1081243	0.83[EUR][1000 genomes]
rs1081244	0.80[EUR][1000 genomes]
rs1081246	0.83[EUR][1000 genomes]
rs1081247	0.83[EUR][1000 genomes]
rs1169471	0.83[EUR][1000 genomes]
rs1169472	0.81[EUR][1000 genomes]
rs1169474	0.81[EUR][1000 genomes]
rs1169475	0.82[EUR][1000 genomes]
rs1169476	0.81[EUR][1000 genomes]
rs1169481	0.82[EUR][1000 genomes]
rs1177610	0.80[EUR][1000 genomes]
rs1177611	0.80[EUR][1000 genomes]
rs1184568	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1184913	0.82[EUR][1000 genomes]
rs1186048	0.82[EUR][1000 genomes]
rs1361608	0.82[EUR][1000 genomes]
rs1752777	0.81[EUR][1000 genomes]
rs1773046	0.81[EUR][1000 genomes]
rs1773062	0.82[EUR][1000 genomes]
rs1935221	0.81[EUR][1000 genomes]
rs1954220	0.81[EUR][1000 genomes]
rs2105313	0.81[EUR][1000 genomes]
rs2105314	0.81[EUR][1000 genomes]
rs2769716	0.82[EUR][1000 genomes]
rs2794624	0.81[EUR][1000 genomes]
rs2794625	0.81[EUR][1000 genomes]
rs2794626	0.81[EUR][1000 genomes]
rs2794627	0.81[EUR][1000 genomes]
rs2794628	0.81[EUR][1000 genomes]
rs2995024	0.80[EUR][1000 genomes]
rs6474978	0.84[EUR][1000 genomes]
rs6474979	0.83[EUR][1000 genomes]
rs7028328	0.80[EUR][1000 genomes]
rs770190	0.83[EUR][1000 genomes]
rs770192	0.81[EUR][1000 genomes]
rs770193	0.84[EUR][1000 genomes]
rs770194	0.81[EUR][1000 genomes]
rs770195	0.80[EUR][1000 genomes]
rs770197	0.84[EUR][1000 genomes]
rs770198	0.82[EUR][1000 genomes]
rs770199	0.80[EUR][1000 genomes]
rs770201	0.80[EUR][1000 genomes]
rs770202	0.80[EUR][1000 genomes]
rs770203	0.84[EUR][1000 genomes]
rs770204	0.82[EUR][1000 genomes]
rs770205	0.82[EUR][1000 genomes]
rs770206	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7860463	0.81[EUR][1000 genomes]
rs9406546	0.81[EUR][1000 genomes]
rs9407665	0.80[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	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	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

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15857800-15885400	Weak transcription	Primary hematopoietic stem cells	blood
2	chr9:15877000-15903400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr9:15877400-15885800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr9:15877600-15888400	Weak transcription	Pancreas	Pancrea
5	chr9:15879000-15885400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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