Variant report

Variant	rs35185476
Chromosome Location	chr13:63060293-63060294
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs12428082	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12428375	0.95[EUR][1000 genomes]
rs12428560	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12429317	0.95[EUR][1000 genomes]
rs12429390	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12429397	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12429424	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12431026	0.95[EUR][1000 genomes]
rs12431035	0.95[EUR][1000 genomes]
rs12431064	0.95[EUR][1000 genomes]
rs12862055	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12864625	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12867188	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12870231	0.95[EUR][1000 genomes]
rs12870258	0.93[EUR][1000 genomes]
rs12870727	0.85[EUR][1000 genomes]
rs12870826	0.91[EUR][1000 genomes]
rs12870935	0.85[EUR][1000 genomes]
rs12870965	0.81[EUR][1000 genomes]
rs12871366	0.95[EUR][1000 genomes]
rs12871694	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12872004	0.95[EUR][1000 genomes]
rs12875690	0.81[EUR][1000 genomes]
rs12875940	0.95[EUR][1000 genomes]
rs12876207	0.95[EUR][1000 genomes]
rs12876281	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12876343	0.91[EUR][1000 genomes]
rs12876465	0.95[EUR][1000 genomes]
rs12876620	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12876700	0.95[EUR][1000 genomes]
rs12876997	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12877105	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12877223	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12877330	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1336141	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17061308	0.95[EUR][1000 genomes]
rs17298039	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs34824349	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs34909131	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35491594	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35869046	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4438182	0.95[EUR][1000 genomes]
rs4883682	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4884420	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4884421	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4884422	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4884423	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs71439933	0.95[EUR][1000 genomes]
rs71439935	0.95[EUR][1000 genomes]
rs71439947	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs71439948	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs71439955	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1038992	chr13:62827929-63369497	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv541795	chr13:62827929-63369497	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1038215	chr13:62836702-63405446	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr13:63057800-63062200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr13:63058000-63062200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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