Variant report

Variant	rs10472152
Chromosome Location	chr5:29202363-29202364
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:29195975..29198561-chr5:29201740..29203808,2	MCF-7	breast:

Extended variants
information (count: 122 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:113)

rs_ID	r²[population]
rs10037010	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10037061	0.87[ASN][1000 genomes]
rs10038700	0.87[ASN][1000 genomes]
rs10039602	0.87[ASN][1000 genomes]
rs10039668	0.87[ASN][1000 genomes]
rs10039689	0.87[ASN][1000 genomes]
rs10039720	0.87[ASN][1000 genomes]
rs10040911	0.87[ASN][1000 genomes]
rs10042518	0.87[ASN][1000 genomes]
rs10045742	0.87[ASN][1000 genomes]
rs10050492	0.87[ASN][1000 genomes]
rs10051008	0.83[ASN][1000 genomes]
rs10056451	0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10056682	0.87[ASN][1000 genomes]
rs10057831	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10057922	0.87[ASN][1000 genomes]
rs10058093	0.87[ASN][1000 genomes]
rs10058284	0.87[ASN][1000 genomes]
rs10060554	0.83[ASN][1000 genomes]
rs10064419	0.83[ASN][1000 genomes]
rs10064605	0.87[ASN][1000 genomes]
rs10064724	0.87[ASN][1000 genomes]
rs10064739	0.87[ASN][1000 genomes]
rs10064857	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10064882	0.87[ASN][1000 genomes]
rs10064929	0.87[ASN][1000 genomes]
rs10064947	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10065134	0.87[ASN][1000 genomes]
rs10066074	0.87[ASN][1000 genomes]
rs10066078	0.87[ASN][1000 genomes]
rs10066277	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10067351	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10068481	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10072535	0.87[ASN][1000 genomes]
rs10072665	0.83[ASN][1000 genomes]
rs10072954	0.87[ASN][1000 genomes]
rs10072999	0.87[ASN][1000 genomes]
rs10073201	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10074755	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10079566	0.83[ASN][1000 genomes]
rs10079924	0.87[ASN][1000 genomes]
rs10080202	0.87[ASN][1000 genomes]
rs1031855	0.83[ASN][1000 genomes]
rs10472151	0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10472154	0.87[ASN][1000 genomes]
rs10472669	0.83[ASN][1000 genomes]
rs10472678	0.87[ASN][1000 genomes]
rs10472680	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10472681	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10472682	0.83[ASN][1000 genomes]
rs10472683	0.86[ASN][1000 genomes]
rs13157869	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13164231	0.87[ASN][1000 genomes]
rs13182294	0.87[ASN][1000 genomes]
rs13356879	0.87[ASN][1000 genomes]
rs13359197	0.87[ASN][1000 genomes]
rs1478863	0.87[ASN][1000 genomes]
rs1478865	0.83[ASN][1000 genomes]
rs1478866	0.83[ASN][1000 genomes]
rs28637428	0.87[ASN][1000 genomes]
rs34228856	0.81[ASN][1000 genomes]
rs34302105	0.87[ASN][1000 genomes]
rs34426391	0.87[ASN][1000 genomes]
rs34687289	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs34979719	0.87[ASN][1000 genomes]
rs35746880	0.87[ASN][1000 genomes]
rs35977446	0.80[ASN][1000 genomes]
rs4130798	0.87[ASN][1000 genomes]
rs4130799	0.87[ASN][1000 genomes]
rs4130800	0.87[ASN][1000 genomes]
rs4354055	0.83[ASN][1000 genomes]
rs4389701	0.83[ASN][1000 genomes]
rs4398647	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4484450	0.83[ASN][1000 genomes]
rs4568373	0.83[ASN][1000 genomes]
rs4587086	0.83[ASN][1000 genomes]
rs4590191	0.83[ASN][1000 genomes]
rs4593276	0.91[ASN][1000 genomes]
rs4631192	0.87[ASN][1000 genomes]
rs4867164	0.83[ASN][1000 genomes]
rs62352828	0.87[ASN][1000 genomes]
rs62352850	0.87[ASN][1000 genomes]
rs62352851	0.87[ASN][1000 genomes]
rs6450671	0.83[ASN][1000 genomes]
rs6450673	0.87[ASN][1000 genomes]
rs6450674	0.83[ASN][1000 genomes]
rs6450675	0.83[ASN][1000 genomes]
rs6866060	0.87[ASN][1000 genomes]
rs6867116	0.83[ASN][1000 genomes]
rs6873017	0.83[ASN][1000 genomes]
rs6873888	0.87[ASN][1000 genomes]
rs6876144	0.83[ASN][1000 genomes]
rs6885342	0.87[ASN][1000 genomes]
rs6895131	0.83[ASN][1000 genomes]
rs7444084	0.87[ASN][1000 genomes]
rs7446320	0.83[ASN][1000 genomes]
rs7714444	0.87[ASN][1000 genomes]
rs7714882	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7715935	0.87[ASN][1000 genomes]
rs7718672	0.80[ASN][1000 genomes]
rs7722678	0.87[ASN][1000 genomes]
rs7731764	0.87[ASN][1000 genomes]
rs7732730	0.83[ASN][1000 genomes]
rs7732750	0.87[ASN][1000 genomes]
rs7732811	0.87[ASN][1000 genomes]
rs9292300	0.83[ASN][1000 genomes]
rs9292307	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs9292311	0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs9292312	0.87[ASN][1000 genomes]
rs9292314	0.87[ASN][1000 genomes]
rs9986176	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9986231	0.87[ASN][1000 genomes]
rs9986285	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 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	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
5	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
6	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
7	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
8	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
9	nsv880414	chr5:29194872-29495564	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 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	chr5:29202200-29211000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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