Variant report

Variant	rs10042518
Chromosome Location	chr5:29183913-29183914
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 145 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:134)

rs_ID	r²[population]
rs10037010	1.00[ASN][1000 genomes]
rs10037061	1.00[ASN][1000 genomes]
rs10038700	1.00[ASN][1000 genomes]
rs10039602	1.00[ASN][1000 genomes]
rs10039668	1.00[ASN][1000 genomes]
rs10039689	1.00[ASN][1000 genomes]
rs10039720	1.00[ASN][1000 genomes]
rs10040911	1.00[ASN][1000 genomes]
rs10045742	1.00[ASN][1000 genomes]
rs10050492	1.00[ASN][1000 genomes]
rs10051008	0.96[ASN][1000 genomes]
rs10056451	1.00[ASN][1000 genomes]
rs10056682	1.00[ASN][1000 genomes]
rs10057831	1.00[ASN][1000 genomes]
rs10057922	1.00[ASN][1000 genomes]
rs10058093	1.00[ASN][1000 genomes]
rs10058226	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10058284	1.00[ASN][1000 genomes]
rs10060554	0.96[ASN][1000 genomes]
rs10064419	0.96[ASN][1000 genomes]
rs10064605	1.00[ASN][1000 genomes]
rs10064724	1.00[ASN][1000 genomes]
rs10064739	1.00[ASN][1000 genomes]
rs10064857	1.00[ASN][1000 genomes]
rs10064882	1.00[ASN][1000 genomes]
rs10064929	1.00[ASN][1000 genomes]
rs10064947	1.00[ASN][1000 genomes]
rs10065134	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10065602	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10066074	1.00[ASN][1000 genomes]
rs10066078	1.00[ASN][1000 genomes]
rs10066277	1.00[ASN][1000 genomes]
rs10068481	1.00[ASN][1000 genomes]
rs10071241	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10072095	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10072535	1.00[ASN][1000 genomes]
rs10072665	0.96[ASN][1000 genomes]
rs10072954	1.00[ASN][1000 genomes]
rs10072999	1.00[ASN][1000 genomes]
rs10073201	1.00[ASN][1000 genomes]
rs10074755	1.00[ASN][1000 genomes]
rs10079566	0.96[ASN][1000 genomes]
rs10079924	1.00[ASN][1000 genomes]
rs10080202	1.00[ASN][1000 genomes]
rs1031855	0.96[ASN][1000 genomes]
rs10472145	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10472151	1.00[ASN][1000 genomes]
rs10472152	0.87[ASN][1000 genomes]
rs10472154	1.00[ASN][1000 genomes]
rs10472669	0.96[ASN][1000 genomes]
rs10472678	1.00[ASN][1000 genomes]
rs10472680	1.00[ASN][1000 genomes]
rs10472681	1.00[ASN][1000 genomes]
rs10472682	0.96[ASN][1000 genomes]
rs10472683	0.91[ASN][1000 genomes]
rs11742838	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12109506	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12697209	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13157869	0.96[ASN][1000 genomes]
rs13164231	1.00[ASN][1000 genomes]
rs13182294	1.00[ASN][1000 genomes]
rs13356879	1.00[ASN][1000 genomes]
rs13357238	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13359197	1.00[ASN][1000 genomes]
rs1478863	1.00[ASN][1000 genomes]
rs1478865	0.96[ASN][1000 genomes]
rs1478866	0.96[ASN][1000 genomes]
rs1587207	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28637428	1.00[ASN][1000 genomes]
rs309666	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs309670	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34214261	0.83[ASN][1000 genomes]
rs34302105	1.00[ASN][1000 genomes]
rs34426391	1.00[ASN][1000 genomes]
rs34464775	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs34687289	1.00[ASN][1000 genomes]
rs34979719	1.00[ASN][1000 genomes]
rs35506895	0.83[ASN][1000 genomes]
rs35746880	1.00[ASN][1000 genomes]
rs35977446	0.92[ASN][1000 genomes]
rs4130798	1.00[ASN][1000 genomes]
rs4130799	1.00[ASN][1000 genomes]
rs4130800	1.00[ASN][1000 genomes]
rs4354055	0.96[ASN][1000 genomes]
rs4374768	0.91[ASN][1000 genomes]
rs4389701	0.96[ASN][1000 genomes]
rs4398647	1.00[ASN][1000 genomes]
rs4484450	0.96[ASN][1000 genomes]
rs4568373	0.96[ASN][1000 genomes]
rs4587086	0.96[ASN][1000 genomes]
rs4590191	0.96[ASN][1000 genomes]
rs4593276	0.96[ASN][1000 genomes]
rs4631192	1.00[ASN][1000 genomes]
rs4867164	0.96[ASN][1000 genomes]
rs62352828	1.00[ASN][1000 genomes]
rs62352850	1.00[ASN][1000 genomes]
rs62352851	1.00[ASN][1000 genomes]
rs6450669	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6450670	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6450671	0.96[ASN][1000 genomes]
rs6450672	0.87[ASN][1000 genomes]
rs6450673	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6450674	0.96[ASN][1000 genomes]
rs6450675	0.96[ASN][1000 genomes]
rs6866060	1.00[ASN][1000 genomes]
rs6867116	0.96[ASN][1000 genomes]
rs6873017	0.96[ASN][1000 genomes]
rs6873888	1.00[ASN][1000 genomes]
rs6876144	0.96[ASN][1000 genomes]
rs6885342	1.00[ASN][1000 genomes]
rs6895131	0.96[ASN][1000 genomes]
rs6899088	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7444084	1.00[ASN][1000 genomes]
rs7446320	0.96[ASN][1000 genomes]
rs7701404	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7714444	1.00[ASN][1000 genomes]
rs7714882	1.00[ASN][1000 genomes]
rs7715935	1.00[ASN][1000 genomes]
rs7718672	0.92[ASN][1000 genomes]
rs7722678	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7731764	1.00[ASN][1000 genomes]
rs7732730	0.96[ASN][1000 genomes]
rs7732750	1.00[ASN][1000 genomes]
rs7732811	1.00[ASN][1000 genomes]
rs7733592	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7737230	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9292300	0.96[ASN][1000 genomes]
rs9292307	1.00[ASN][1000 genomes]
rs9292311	1.00[ASN][1000 genomes]
rs9292312	1.00[ASN][1000 genomes]
rs9292314	1.00[ASN][1000 genomes]
rs9986176	1.00[ASN][1000 genomes]
rs9986231	1.00[ASN][1000 genomes]
rs9986285	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023990	chr5:28917253-29220447	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	esv3528360	chr5:29069255-29548659	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
3	esv3528361	chr5:29069255-29548659	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
4	nsv1022253	chr5:29076460-29195987	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
5	nsv1016603	chr5:29102713-29843965	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
6	nsv537712	chr5:29102713-29843965	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
7	nsv1030526	chr5:29125802-29204186	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
8	nsv964827	chr5:29138557-29198352	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
9	nsv525210	chr5:29176529-29194872	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv1031329	chr5:29177677-29760923	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
11	nsv537713	chr5:29177677-29760923	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:29177000-29185800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links