Variant report

Variant	rs10911892
Chromosome Location	chr1:186569429-186569430
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 76 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10798051	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10798052	0.84[AFR][1000 genomes]
rs10911877	1.00[CEU][hapmap];0.91[CHB][hapmap];0.86[YRI][hapmap];0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10911878	0.83[CEU][hapmap];0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10911888	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10911890	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10911895	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10911898	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11580808	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11582183	1.00[CEU][hapmap];0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11804161	0.81[ASN][1000 genomes]
rs11805124	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11806329	0.81[ASN][1000 genomes]
rs11806663	0.83[ASN][1000 genomes]
rs11807318	0.81[ASN][1000 genomes]
rs11807443	0.81[ASN][1000 genomes]
rs11808165	0.83[ASN][1000 genomes]
rs11808900	0.83[JPT][hapmap]
rs11809088	0.83[ASN][1000 genomes]
rs11810534	0.86[JPT][hapmap]
rs11811335	0.83[ASN][1000 genomes]
rs12087470	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12093901	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12402521	1.00[CEU][hapmap];0.80[CHB][hapmap];0.87[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12723621	0.82[JPT][hapmap]
rs12726528	0.81[ASN][1000 genomes]
rs12726764	0.81[ASN][1000 genomes]
rs12728706	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12747991	0.81[ASN][1000 genomes]
rs12750371	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12751255	0.82[ASN][1000 genomes]
rs12753223	0.81[ASN][1000 genomes]
rs16825675	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1799957	1.00[CEU][hapmap];0.84[CHB][hapmap];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1929092	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2024761	1.00[CEU][hapmap];0.80[CHB][hapmap];0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2180167	0.95[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2207727	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2383508	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34200789	0.81[ASN][1000 genomes]
rs34396375	0.97[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34783173	0.80[ASN][1000 genomes]
rs35240980	0.81[ASN][1000 genomes]
rs35643079	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs36016361	0.81[ASN][1000 genomes]
rs36030781	0.81[ASN][1000 genomes]
rs36105782	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs3844242	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3901950	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4140432	0.83[JPT][hapmap]
rs4140433	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4567244	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs59547074	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6425035	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6425038	0.84[EUR][1000 genomes]
rs6659683	1.00[CEU][hapmap];0.87[AMR][1000 genomes]
rs6666413	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6666813	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6672836	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6675505	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6677346	1.00[CEU][hapmap];0.91[CHB][hapmap];0.96[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6680252	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6689065	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6689727	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6694957	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs71634175	0.83[ASN][1000 genomes]
rs71634176	0.83[ASN][1000 genomes]
rs7518525	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7536199	0.87[AMR][1000 genomes]
rs7539054	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7556360	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1004481	chr1:186095854-186750968	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
2	nsv535223	chr1:186095854-186750968	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
3	nsv832059	chr1:186464932-186639125	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv2762854	chr1:186547101-186847574	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
5	nsv872590	chr1:186557453-187500338	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 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	chr1:186568600-186571000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links