Variant report

Variant	rs73136709
Chromosome Location	chr3:81961898-81961899
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10433513	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10460925	0.81[AMR][1000 genomes]
rs11127744	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11127745	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12631503	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12638592	0.81[ASN][1000 genomes]
rs1524556	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17019364	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17019369	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17019416	0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17019418	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17019431	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs55988714	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56019819	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56028558	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56120615	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60428278	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61156634	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61540531	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61617076	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6765293	0.94[EUR][1000 genomes]
rs6784904	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6791857	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs73134760	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73134764	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73134800	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73134802	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73138733	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73138765	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73138781	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73138782	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73138783	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73140754	0.89[ASN][1000 genomes]
rs7611964	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7612181	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7618777	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7619049	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 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

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:81958000-81963200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr3:81961600-81963000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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