Variant report

Variant	rs6050056
Chromosome Location	chr20:24849861-24849862
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 119 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:111)

rs_ID	r²[population]
rs1029031	1.00[ASN][1000 genomes]
rs1029032	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1029033	1.00[ASN][1000 genomes]
rs11087480	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1113872	1.00[ASN][1000 genomes]
rs1122607	1.00[ASN][1000 genomes]
rs11905160	1.00[ASN][1000 genomes]
rs11906401	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11906511	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1331285	1.00[ASN][1000 genomes]
rs1331290	1.00[ASN][1000 genomes]
rs1411892	1.00[ASN][1000 genomes]
rs1411894	1.00[ASN][1000 genomes]
rs1411895	1.00[ASN][1000 genomes]
rs1831483	1.00[ASN][1000 genomes]
rs1888655	1.00[ASN][1000 genomes]
rs2064404	0.85[CEU][hapmap];1.00[CHB][hapmap]
rs2150644	0.84[EUR][1000 genomes]
rs4239751	0.85[CEU][hapmap];1.00[CHB][hapmap]
rs4815358	0.86[CEU][hapmap];1.00[CHB][hapmap]
rs4815359	0.86[CEU][hapmap];1.00[CHB][hapmap]
rs55702326	1.00[ASN][1000 genomes]
rs56053259	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56106395	1.00[ASN][1000 genomes]
rs56148678	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56179484	1.00[ASN][1000 genomes]
rs56249107	0.91[EUR][1000 genomes]
rs56299926	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs56406017	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs58353086	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6036915	1.00[ASN][1000 genomes]
rs6036939	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6036940	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6036943	1.00[ASN][1000 genomes]
rs6036946	1.00[ASN][1000 genomes]
rs6036948	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6036951	1.00[ASN][1000 genomes]
rs6036955	1.00[ASN][1000 genomes]
rs6036967	1.00[ASN][1000 genomes]
rs6036968	1.00[ASN][1000 genomes]
rs6036969	1.00[ASN][1000 genomes]
rs6036970	1.00[ASN][1000 genomes]
rs6036971	1.00[ASN][1000 genomes]
rs6036972	1.00[ASN][1000 genomes]
rs6050000	1.00[ASN][1000 genomes]
rs6050007	1.00[ASN][1000 genomes]
rs6050026	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6050051	1.00[ASN][1000 genomes]
rs6050052	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6050058	1.00[ASN][1000 genomes]
rs6050066	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6050070	1.00[ASN][1000 genomes]
rs6050073	1.00[ASN][1000 genomes]
rs6050074	1.00[ASN][1000 genomes]
rs6050111	1.00[ASN][1000 genomes]
rs6050114	1.00[ASN][1000 genomes]
rs6050115	1.00[ASN][1000 genomes]
rs6050116	1.00[ASN][1000 genomes]
rs6050117	1.00[ASN][1000 genomes]
rs6050119	1.00[ASN][1000 genomes]
rs6050120	1.00[ASN][1000 genomes]
rs6050121	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6050123	0.91[AMR][1000 genomes]
rs6050124	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6050199	0.85[CEU][hapmap]
rs6076288	0.92[EUR][1000 genomes]
rs6076289	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6076290	1.00[ASN][1000 genomes]
rs6076291	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6076292	1.00[ASN][1000 genomes]
rs6076293	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6083628	1.00[ASN][1000 genomes]
rs6083638	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6083639	0.90[EUR][1000 genomes]
rs6083645	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6083646	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6083647	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6083648	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6083649	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6083650	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6083651	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6083653	0.91[EUR][1000 genomes]
rs6083656	1.00[ASN][1000 genomes]
rs6083657	0.91[EUR][1000 genomes]
rs6083658	1.00[ASN][1000 genomes]
rs6083697	0.85[CEU][hapmap];1.00[CHB][hapmap]
rs6083714	0.84[CEU][hapmap];1.00[CHB][hapmap]
rs6106957	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6106963	1.00[ASN][1000 genomes]
rs6106965	0.85[AMR][1000 genomes]
rs6106967	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6106968	1.00[ASN][1000 genomes]
rs6114893	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6114915	1.00[ASN][1000 genomes]
rs6114918	1.00[ASN][1000 genomes]
rs6114921	1.00[ASN][1000 genomes]
rs62215832	1.00[ASN][1000 genomes]
rs6515535	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6515538	1.00[ASN][1000 genomes]
rs73108128	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73110258	0.83[EUR][1000 genomes]
rs73110260	0.83[EUR][1000 genomes]
rs761368	0.85[CEU][hapmap];1.00[CHB][hapmap]
rs765834	0.86[CEU][hapmap];1.00[CHB][hapmap]
rs8114708	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs8114760	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs8119191	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs8120506	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs8123541	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs914308	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs914309	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1061412	chr20:24629468-24887869	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv544216	chr20:24629468-24887869	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1061455	chr20:24733120-24861801	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv544218	chr20:24733120-24861801	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1062140	chr20:24807962-25304054	Strong transcription Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
6	nsv544219	chr20:24807962-25304054	Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Active TSS Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
7	nsv1056345	chr20:24819570-25168159	Flanking Active TSS Bivalent Enhancer Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
8	nsv1055341	chr20:24848416-25302271	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 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	chr20:24849600-24851400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr20:24849800-24851400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links