Variant report

Variant	rs73149803
Chromosome Location	chr3:144069598-144069599
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs1019951	1.00[ASN][1000 genomes]
rs10490849	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10490850	0.82[EUR][1000 genomes]
rs10490852	0.82[EUR][1000 genomes]
rs1118666	0.91[ASN][1000 genomes]
rs11923441	0.82[EUR][1000 genomes]
rs11926486	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11928581	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12054182	0.91[ASN][1000 genomes]
rs1526567	0.91[ASN][1000 genomes]
rs1608999	0.91[ASN][1000 genomes]
rs16855353	0.82[EUR][1000 genomes]
rs17208351	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1918059	0.91[ASN][1000 genomes]
rs197836	0.90[ASN][1000 genomes]
rs197840	0.97[ASN][1000 genomes]
rs197856	0.97[ASN][1000 genomes]
rs2082509	0.91[ASN][1000 genomes]
rs2117005	0.88[ASN][1000 genomes]
rs4141532	0.91[ASN][1000 genomes]
rs4681103	0.91[ASN][1000 genomes]
rs4681255	0.93[EUR][1000 genomes]
rs73147701	1.00[EUR][1000 genomes]
rs73149804	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73149806	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73149810	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73149813	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73149814	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73149815	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73149816	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73149821	0.82[EUR][1000 genomes]
rs73149823	0.82[EUR][1000 genomes]
rs73149824	0.82[EUR][1000 genomes]
rs73149840	0.82[EUR][1000 genomes]
rs73149841	0.82[EUR][1000 genomes]
rs73149845	0.82[EUR][1000 genomes]
rs73149848	0.82[EUR][1000 genomes]
rs7619281	0.88[ASN][1000 genomes]
rs979000	0.91[ASN][1000 genomes]
rs9835986	0.91[ASN][1000 genomes]
rs9842442	0.88[ASN][1000 genomes]
rs9878391	0.91[ASN][1000 genomes]
rs9880662	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010117	chr3:143750590-144093775	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv536748	chr3:143750590-144093775	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv532633	chr3:143802417-144440646	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv877570	chr3:143853149-144123401	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1011685	chr3:143959237-144218424	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv536751	chr3:143959237-144218424	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv591928	chr3:144050897-144822081	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:144064400-144069800	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr3:144064600-144069600	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr3:144068400-144069600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr3:144068400-144069800	Enhancers	Fetal Lung	lung
5	chr3:144068600-144069600	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr3:144068600-144070600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr3:144069000-144070000	Active TSS	Fetal Kidney	kidney
8	chr3:144069200-144069800	Enhancers	Liver	Liver
9	chr3:144069400-144071600	Enhancers	Primary monocytes fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links