Variant report

Variant	rs9812505
Chromosome Location	chr3:81922179-81922180
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs13314900	0.81[EUR][1000 genomes]
rs1524556	0.81[ASN][1000 genomes]
rs17019364	0.85[ASN][1000 genomes]
rs17019369	0.85[ASN][1000 genomes]
rs1851922	0.86[EUR][1000 genomes]
rs1851924	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1973802	0.83[EUR][1000 genomes]
rs2316043	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2680275	0.84[EUR][1000 genomes]
rs61156634	0.81[ASN][1000 genomes]
rs61540531	0.85[ASN][1000 genomes]
rs62267150	0.82[EUR][1000 genomes]
rs6765293	0.82[ASN][1000 genomes]
rs6768673	0.86[EUR][1000 genomes]
rs6778413	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6785740	0.81[EUR][1000 genomes]
rs6791629	0.83[EUR][1000 genomes]
rs6791857	0.85[ASN][1000 genomes]
rs6798822	0.84[EUR][1000 genomes]
rs6804613	0.83[EUR][1000 genomes]
rs7611917	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7635332	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7644425	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9812141	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9813371	0.82[EUR][1000 genomes]
rs9825400	0.82[EUR][1000 genomes]
rs9827558	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9831301	0.82[EUR][1000 genomes]
rs9835279	0.86[EUR][1000 genomes]
rs9838598	0.83[EUR][1000 genomes]
rs9851559	0.82[EUR][1000 genomes]
rs9870979	0.83[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	nsv999992	chr3:81693662-82015969	Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv536605	chr3:81693662-82015969	Flanking Active TSS Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv441830	chr3:81909338-81923746	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:81914000-81927000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr3:81920000-81922800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr3:81921400-81922600	Enhancers	NHDF-Ad	bronchial
4	chr3:81922000-81926000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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