Variant report

Variant	rs1865955
Chromosome Location	chr10:118837990-118837991
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:118832679..118834580-chr10:118836577..118838384,2	MCF-7	breast:

Extended variants
information (count: 32 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10128516	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10749237	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10787751	0.91[EUR][1000 genomes]
rs10787760	0.88[ASW][hapmap];0.81[JPT][hapmap];0.84[LWK][hapmap];0.91[MKK][hapmap];0.95[YRI][hapmap];0.86[AFR][1000 genomes]
rs10886037	0.91[EUR][1000 genomes]
rs10886038	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10886040	0.89[EUR][1000 genomes]
rs11197887	0.90[EUR][1000 genomes]
rs11197892	0.88[EUR][1000 genomes]
rs11197899	0.88[EUR][1000 genomes]
rs12244454	0.95[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12268087	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1865954	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1871345	0.81[EUR][1000 genomes]
rs1898349	0.88[EUR][1000 genomes]
rs1898351	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1898357	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1905538	0.86[MEX][hapmap]
rs1947798	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2118207	0.86[MEX][hapmap]
rs2420308	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3847479	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4752028	0.92[CEU][hapmap];0.93[TSI][hapmap];0.90[EUR][1000 genomes]
rs6585429	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7069235	0.87[EUR][1000 genomes]
rs7072663	0.89[EUR][1000 genomes]
rs7078823	0.90[EUR][1000 genomes]
rs7085083	0.93[EUR][1000 genomes]
rs7087662	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7093171	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7917897	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832002	chr10:118797070-119005840	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	24 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs1865955	DKFZp781N1041	cis	multi-tissue	Pritchard
rs1865955	KIAA1598	cis	Whole Blood	GTEx
rs1865955	OR5K4	trans	parietal	SCAN
rs1865955	KIAA1598	cis	multi-tissue	Pritchard
rs1865955	KCNK18	cis	parietal	SCAN
rs1865955	WDR11	cis	parietal	SCAN

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:118837600-118838000	Enhancers	HMEC	breast
2	chr10:118837800-118838200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr10:118837800-118838200	Enhancers	Gastric	stomach

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