Variant report

Variant	rs71478670
Chromosome Location	chr15:58780802-58780803
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10518978	0.81[ASN][1000 genomes]
rs11634902	0.93[ASN][1000 genomes]
rs12591216	0.92[ASN][1000 genomes]
rs12591624	0.87[ASN][1000 genomes]
rs12592407	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12593736	0.81[ASN][1000 genomes]
rs12593880	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12594222	0.87[ASN][1000 genomes]
rs12595191	0.81[ASN][1000 genomes]
rs12900891	0.81[ASN][1000 genomes]
rs12902119	0.81[ASN][1000 genomes]
rs12903955	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12906459	0.81[ASN][1000 genomes]
rs12908427	1.00[ASN][1000 genomes]
rs12910028	0.91[ASN][1000 genomes]
rs12910602	0.87[ASN][1000 genomes]
rs12913605	0.81[ASN][1000 genomes]
rs16940338	0.81[ASN][1000 genomes]
rs17190580	0.87[ASN][1000 genomes]
rs17190587	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2414581	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28478642	0.91[ASN][1000 genomes]
rs28713618	0.85[ASN][1000 genomes]
rs2899630	0.96[ASN][1000 genomes]
rs34053638	0.81[ASN][1000 genomes]
rs34297592	0.81[ASN][1000 genomes]
rs34570549	0.81[ASN][1000 genomes]
rs34577128	0.87[ASN][1000 genomes]
rs34744603	0.81[ASN][1000 genomes]
rs35633916	0.81[ASN][1000 genomes]
rs35732576	0.81[ASN][1000 genomes]
rs35771822	0.96[ASN][1000 genomes]
rs35795657	0.96[ASN][1000 genomes]
rs4775053	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6494009	0.81[ASN][1000 genomes]
rs6494010	0.81[ASN][1000 genomes]
rs6494011	0.81[ASN][1000 genomes]
rs71478668	0.87[ASN][1000 genomes]
rs71478671	0.98[ASN][1000 genomes]
rs71478672	0.95[ASN][1000 genomes]
rs7162384	0.87[ASN][1000 genomes]
rs7162603	0.87[ASN][1000 genomes]
rs7172556	0.81[ASN][1000 genomes]
rs7174539	0.81[ASN][1000 genomes]
rs8029592	0.96[ASN][1000 genomes]
rs8029837	0.96[ASN][1000 genomes]
rs8041525	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051058	chr15:58519922-59092530	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv542401	chr15:58519922-59092530	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv569598	chr15:58552606-58852463	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv1047048	chr15:58701400-58784800	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv3362898	chr15:58705732-58850860	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv1043041	chr15:58744505-58876327	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv904268	chr15:58763678-58803225	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58775600-58781000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
2	chr15:58776600-58782400	Weak transcription	Right Ventricle	heart
3	chr15:58779200-58784000	Weak transcription	Esophagus	oesophagus
4	chr15:58779200-58784000	Weak transcription	Pancreas	Pancrea
5	chr15:58779400-58783400	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr15:58780200-58781400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr15:58780200-58787800	Weak transcription	Fetal Kidney	kidney
8	chr15:58780600-58782000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr15:58780800-58781600	Weak transcription	Primary T cells from cord blood	blood
10	chr15:58780800-58786200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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