Variant report

Variant	rs10489338
Chromosome Location	chr1:209754361-209754362
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:209754061..209755961-chr1:209923961..209926598,2	K562	blood:

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11119308	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11119309	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12058586	1.00[CHB][hapmap];0.82[JPT][hapmap];0.91[ASN][1000 genomes]
rs12069172	0.83[ASN][1000 genomes]
rs12074063	0.91[ASN][1000 genomes]
rs12080730	0.83[ASN][1000 genomes]
rs12094286	0.80[CHB][hapmap];0.81[ASN][1000 genomes]
rs17014758	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17014770	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17014799	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17014808	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17014825	1.00[CEU][hapmap];0.89[CHB][hapmap];0.82[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17014842	0.84[CHB][hapmap];0.81[ASN][1000 genomes]
rs2067744	0.83[ASN][1000 genomes]
rs2072908	0.86[CHB][hapmap];0.83[ASN][1000 genomes]
rs2076225	0.90[CHB][hapmap];0.83[ASN][1000 genomes]
rs60686175	0.84[ASN][1000 genomes]
rs6663545	0.83[ASN][1000 genomes]
rs6690557	0.95[CHB][hapmap]
rs7512091	0.85[CHB][hapmap];0.84[JPT][hapmap];0.83[ASN][1000 genomes]
rs926385	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9429821	0.95[CHB][hapmap]
rs9429822	0.83[ASN][1000 genomes]
rs9430000	1.00[CHB][hapmap];0.88[JPT][hapmap];0.96[ASN][1000 genomes]
rs9430001	1.00[CHB][hapmap]
rs9430005	0.83[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	nsv999901	chr1:209600631-210205379	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 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	chr1:209751000-209756200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr1:209751000-209756400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:209751000-209756600	Weak transcription	NHLF	lung
4	chr1:209751000-209758600	Weak transcription	HMEC	breast
5	chr1:209753400-209754400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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