Variant report

Variant	rs8032589
Chromosome Location	chr15:41501483-41501484
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:74)

rs_ID	r²[population]
rs10152855	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11070321	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs11070325	0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11855102	0.89[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs11858115	0.80[JPT][hapmap]
rs11858678	0.89[CHB][hapmap];0.80[JPT][hapmap]
rs16971693	0.88[CEU][hapmap];0.94[CHB][hapmap];0.95[JPT][hapmap];0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs16971700	0.92[AMR][1000 genomes];0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1866400	0.88[CEU][hapmap];0.94[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1971131	0.94[CHB][hapmap];0.80[JPT][hapmap];0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2083239	0.81[ASN][1000 genomes]
rs2164996	0.80[JPT][hapmap]
rs28493237	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28495204	0.91[AMR][1000 genomes];0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2899013	0.83[ASN][1000 genomes]
rs2918462	0.89[CHB][hapmap];0.80[JPT][hapmap]
rs41442144	0.92[AMR][1000 genomes];0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4258585	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs551482	0.80[ASN][1000 genomes]
rs55756301	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56082289	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56837771	0.85[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs57943533	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs58083671	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs58644012	0.82[ASN][1000 genomes]
rs59389433	0.94[AMR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs59616518	0.89[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs59691280	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs60249025	0.91[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs60422198	0.91[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs61495227	0.91[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs61586152	0.80[ASN][1000 genomes]
rs6492988	0.85[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs6492991	0.88[ASN][1000 genomes]
rs6492992	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6492993	0.83[CHB][hapmap];0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs6492997	0.80[JPT][hapmap]
rs66471237	0.91[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs66510055	0.91[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs66602495	0.80[ASN][1000 genomes]
rs67531333	0.89[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs68133575	0.82[ASN][1000 genomes]
rs690733	0.89[CHB][hapmap];0.80[JPT][hapmap];0.80[ASN][1000 genomes]
rs691702	0.80[ASN][1000 genomes]
rs7165931	0.85[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs7166205	0.88[ASN][1000 genomes]
rs7166905	0.86[ASN][1000 genomes]
rs7170049	0.89[CHB][hapmap];0.80[JPT][hapmap];0.83[ASN][1000 genomes]
rs7170913	0.91[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7173086	0.89[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs7175912	0.80[JPT][hapmap]
rs7178840	0.88[CEU][hapmap];0.94[CHB][hapmap];0.95[JPT][hapmap];0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7179231	0.88[CEU][hapmap];0.94[CHB][hapmap];0.95[JPT][hapmap];0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7179676	0.85[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7179969	0.88[CEU][hapmap];0.94[CHB][hapmap];0.95[JPT][hapmap];0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72737765	0.80[ASN][1000 genomes]
rs73396329	0.80[ASN][1000 genomes]
rs73396336	0.81[ASN][1000 genomes]
rs8023638	0.83[ASN][1000 genomes]
rs8026858	0.94[CHB][hapmap];0.81[JPT][hapmap];0.91[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs8029792	0.82[ASN][1000 genomes]
rs8035252	0.88[CEU][hapmap];0.94[CHB][hapmap];0.95[JPT][hapmap];0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8038834	0.94[CHB][hapmap];0.80[JPT][hapmap];0.91[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs8039014	0.94[CHB][hapmap];0.81[JPT][hapmap]
rs8039915	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8039934	0.94[CHB][hapmap];0.80[JPT][hapmap];0.91[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs8043253	0.88[CHB][hapmap];0.94[JPT][hapmap]
rs909023	0.88[CEU][hapmap];0.94[CHB][hapmap];0.95[JPT][hapmap];0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs909024	0.87[CEU][hapmap];0.89[CHB][hapmap];0.82[JPT][hapmap];0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs909025	0.93[CEU][hapmap];0.89[CHB][hapmap];0.95[JPT][hapmap];0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9972345	0.85[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs9972349	0.89[CHB][hapmap];0.85[JPT][hapmap];0.83[ASN][1000 genomes]
rs9972622	0.83[ASN][1000 genomes]
rs9972623	0.81[ASN][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	nsv457120	chr15:41410705-41546631	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv569231	chr15:41410705-41546631	Weak transcription ZNF genes & repeats Active TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv1039906	chr15:41476209-41518976	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:41500200-41501600	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr15:41500400-41501600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr15:41500800-41501600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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