Variant report

Variant	rs28493166
Chromosome Location	chr15:93306644-93306645
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs11074104	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12594947	0.82[AMR][1000 genomes]
rs12910258	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs28476168	0.95[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs28569165	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs28645459	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs28711427	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4072158	0.85[AMR][1000 genomes]
rs4072159	0.83[AMR][1000 genomes]
rs4313764	0.82[AMR][1000 genomes]
rs6496991	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs67463648	0.82[AMR][1000 genomes]
rs7167019	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7167390	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7167395	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7167779	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7168245	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7168253	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7169034	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7171052	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7171375	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7172746	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7173021	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7173418	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7173890	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7174203	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7174856	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7174939	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7177154	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7178715	0.82[AMR][1000 genomes]
rs7183797	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7494848	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs8031203	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs8032507	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs8038332	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9302359	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9744428	0.84[AMR][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	nsv904499	chr15:92914795-93472582	Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	163 gene(s)	inside rSNPs	diseases
2	nsv948738	chr15:93070742-93728147	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	169 gene(s)	inside rSNPs	diseases
3	nsv1049490	chr15:93134405-93591660	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	151 gene(s)	inside rSNPs	diseases
4	nsv1042292	chr15:93286333-93374887	Flanking Active TSS Weak transcription Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
5	nsv984199	chr15:93288362-93381522	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
6	nsv94522	chr15:93306419-93316316	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:93295800-93323200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr15:93304800-93344800	Weak transcription	Aorta	Aorta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links