Variant report

Variant	rs7501207
Chromosome Location	chr16:31351552-31351553
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs10747210	0.81[ASN][1000 genomes]
rs10782004	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11150610	0.83[ASN][1000 genomes]
rs11150611	0.82[ASN][1000 genomes]
rs11150612	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11150613	0.82[ASN][1000 genomes]
rs11150617	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11150619	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1143682	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs11574630	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11574631	0.81[ASN][1000 genomes]
rs11642120	0.83[ASN][1000 genomes]
rs11645917	0.83[ASN][1000 genomes]
rs11859274	0.83[ASN][1000 genomes]
rs12444713	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12597154	0.93[ASN][1000 genomes]
rs12923297	0.83[ASN][1000 genomes]
rs12935192	0.83[ASN][1000 genomes]
rs13338928	0.82[ASN][1000 genomes]
rs2230429	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs28372932	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3087796	0.83[ASN][1000 genomes]
rs36100148	0.84[ASN][1000 genomes]
rs3925074	0.87[ASN][1000 genomes]
rs3925075	0.87[ASN][1000 genomes]
rs4075052	0.87[ASN][1000 genomes]
rs4077810	0.81[ASN][1000 genomes]
rs41440449	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4261553	0.87[ASN][1000 genomes]
rs4359460	0.87[ASN][1000 genomes]
rs4411512	0.87[ASN][1000 genomes]
rs4448960	0.87[ASN][1000 genomes]
rs4450409	0.94[ASN][1000 genomes]
rs4459557	0.82[ASN][1000 genomes]
rs4493054	0.81[ASN][1000 genomes]
rs4506917	0.87[ASN][1000 genomes]
rs4594268	0.83[ASN][1000 genomes]
rs4597342	0.82[ASN][1000 genomes]
rs4608351	0.87[ASN][1000 genomes]
rs4889543	0.83[ASN][1000 genomes]
rs4889647	0.81[ASN][1000 genomes]
rs4889649	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs55742763	0.83[ASN][1000 genomes]
rs55912556	0.89[ASN][1000 genomes]
rs56392848	0.82[ASN][1000 genomes]
rs57202326	0.91[ASN][1000 genomes]
rs59338016	0.89[ASN][1000 genomes]
rs61194152	0.81[ASN][1000 genomes]
rs62051517	0.84[ASN][1000 genomes]
rs7192161	0.81[ASN][1000 genomes]
rs7192375	0.82[ASN][1000 genomes]
rs7195915	0.84[ASN][1000 genomes]
rs7195945	0.84[ASN][1000 genomes]
rs8052324	0.81[ASN][1000 genomes]
rs8058882	0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8060268	0.84[ASN][1000 genomes]
rs8062159	0.95[ASN][1000 genomes]
rs9673398	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9673404	0.87[ASN][1000 genomes]
rs9673405	0.87[ASN][1000 genomes]
rs9673519	0.87[ASN][1000 genomes]
rs9673522	0.87[ASN][1000 genomes]
rs9674009	0.87[ASN][1000 genomes]
rs9888907	0.87[ASN][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	nsv1059459	chr16:31299088-31462251	Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
2	nsv542901	chr16:31299088-31462251	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
3	esv3392534	chr16:31303038-31573066	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	104 gene(s)	inside rSNPs	diseases
4	nsv1058992	chr16:31337455-31414881	Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
5	nsv542902	chr16:31337455-31414881	Weak transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
6	nsv1061980	chr16:31338462-31415471	Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31343000-31400800	Weak transcription	Right Atrium	heart
2	chr16:31350200-31356000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr16:31350200-31356200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr16:31350400-31355800	Weak transcription	Primary T cells fromperipheralblood	blood

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