Variant report

Variant	rs9351847
Chromosome Location	chr6:72434107-72434108
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11965010	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12055765	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12173946	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2220290	0.81[ASN][1000 genomes]
rs2220291	0.91[JPT][hapmap]
rs4707934	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60502272	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62407661	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs62407672	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62408732	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9341336	0.82[ASN][1000 genomes]
rs9342864	0.91[JPT][hapmap]
rs9342866	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9342868	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9350422	0.82[ASN][1000 genomes]
rs9351841	0.91[JPT][hapmap]
rs9351843	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs9358968	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs9358970	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9358971	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9360480	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs9360481	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs9360482	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs9360484	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9360487	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830686	chr6:72336896-72534267	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr6:72421000-72443400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:72430400-72434600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr6:72430800-72436200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr6:72432000-72434800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr6:72432000-72435000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr6:72432000-72437600	Weak transcription	Osteobl	bone
7	chr6:72433800-72435200	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr6:72434000-72434400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr6:72434000-72434400	Weak transcription	Fetal Intestine Large	intestine

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