Variant report

Variant	rs34572897
Chromosome Location	chr1:78979194-78979195
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10489787	1.00[ASN][1000 genomes]
rs12058120	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12082394	1.00[ASN][1000 genomes]
rs12094298	1.00[ASN][1000 genomes]
rs12725125	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12740498	1.00[ASN][1000 genomes]
rs12748050	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1322933	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1322934	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1322935	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28832602	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs33994937	1.00[ASN][1000 genomes]
rs34012602	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34077564	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34490913	0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34528585	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34852041	1.00[ASN][1000 genomes]
rs35123627	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35324676	1.00[ASN][1000 genomes]
rs35978825	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3766346	0.97[ASN][1000 genomes]
rs3766347	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3766348	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3766351	1.00[ASN][1000 genomes]
rs61769118	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6700362	1.00[ASN][1000 genomes]
rs672561	0.97[ASN][1000 genomes]
rs67351117	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72673924	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72673925	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[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	nsv871835	chr1:78528803-79501129	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv870807	chr1:78867347-79032598	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:78977600-78982800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr1:78977600-78987600	Weak transcription	NHDF-Ad	bronchial
3	chr1:78977600-78993200	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr1:78977800-78987800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr1:78978600-78984800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links