Variant report

Variant	rs7322266
Chromosome Location	chr13:29779573-29779574
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 85 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs1029190	1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AMR][1000 genomes]
rs12429003	0.82[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes]
rs1318661	0.86[CEU][hapmap]
rs1335653	0.82[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes]
rs1335654	0.90[AMR][1000 genomes]
rs1335663	0.83[AMR][1000 genomes]
rs1360856	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1360857	0.82[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AMR][1000 genomes]
rs1360858	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs1541133	1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AMR][1000 genomes]
rs1577475	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1577476	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1577478	1.00[JPT][hapmap];0.83[AMR][1000 genomes]
rs1927831	0.83[CEU][hapmap]
rs1927834	0.80[CEU][hapmap]
rs1999717	0.82[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes]
rs2050463	0.82[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes]
rs4098154	1.00[JPT][hapmap];0.84[AMR][1000 genomes]
rs4146404	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs4146405	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs4369507	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4603401	1.00[JPT][hapmap]
rs4769005	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4769006	0.82[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes]
rs4769008	1.00[JPT][hapmap];0.83[AMR][1000 genomes]
rs4769685	0.86[CEU][hapmap]
rs4769686	0.86[CEU][hapmap]
rs4769688	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4769689	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4769692	0.86[CEU][hapmap]
rs4769693	0.84[CEU][hapmap]
rs4769698	0.90[AMR][1000 genomes]
rs4769699	0.88[AMR][1000 genomes]
rs4769702	0.83[AMR][1000 genomes]
rs4769704	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs6490362	0.85[CEU][hapmap]
rs6490365	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6490368	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs6490370	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6490376	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6490377	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6490379	0.90[AMR][1000 genomes]
rs6490380	0.90[AMR][1000 genomes]
rs6490381	0.81[AMR][1000 genomes]
rs7325901	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7328586	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7337839	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs7338024	0.86[CEU][hapmap]
rs7981178	0.82[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes]
rs7981243	0.82[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes]
rs7981300	0.83[AMR][1000 genomes]
rs7981637	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs7982062	0.82[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes]
rs7982077	0.82[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes]
rs7983586	0.85[CEU][hapmap]
rs7984848	0.80[CEU][hapmap]
rs7985145	0.82[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AMR][1000 genomes]
rs7985337	0.84[AMR][1000 genomes]
rs7985374	0.80[CEU][hapmap]
rs7985618	0.80[CEU][hapmap]
rs7988808	0.86[CEU][hapmap]
rs7998019	1.00[JPT][hapmap]
rs7999446	1.00[JPT][hapmap];0.83[AMR][1000 genomes]
rs7999907	0.82[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes]
rs8001430	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs8001681	0.82[CEU][hapmap]
rs9314942	0.82[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes]
rs9314943	0.83[AMR][1000 genomes]
rs9314944	1.00[JPT][hapmap];0.83[AMR][1000 genomes]
rs9508321	0.90[AMR][1000 genomes]
rs9550443	0.83[CEU][hapmap]
rs9550445	0.86[CEU][hapmap]
rs9550453	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs9579292	0.82[JPT][hapmap]
rs9579300	1.00[JPT][hapmap]
rs9579303	0.86[CEU][hapmap]
rs9579306	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9579308	1.00[JPT][hapmap];0.83[AMR][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	nsv533835	chr13:29141132-29962069	Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	esv3406145	chr13:29616606-29917459	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv899957	chr13:29720732-29820422	Weak transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv427927	chr13:29729315-30062054	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv899958	chr13:29752497-29820422	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv899959	chr13:29752497-29832613	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv976	chr13:29759458-29804146	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links