Variant report

Variant	rs56270524
Chromosome Location	chr3:101982378-101982379
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs1072718	0.82[ASN][1000 genomes]
rs11706182	0.82[ASN][1000 genomes]
rs11716644	0.82[ASN][1000 genomes]
rs11918608	0.82[ASN][1000 genomes]
rs11920927	0.82[ASN][1000 genomes]
rs11921270	0.82[ASN][1000 genomes]
rs11922579	0.82[ASN][1000 genomes]
rs11928361	0.82[ASN][1000 genomes]
rs1382788	0.82[ASN][1000 genomes]
rs1585772	0.82[ASN][1000 genomes]
rs1585774	0.82[ASN][1000 genomes]
rs1600328	0.82[ASN][1000 genomes]
rs1600329	0.82[ASN][1000 genomes]
rs1842175	0.82[ASN][1000 genomes]
rs1904343	0.82[ASN][1000 genomes]
rs1993928	0.82[ASN][1000 genomes]
rs2086269	0.82[ASN][1000 genomes]
rs2100993	0.82[ASN][1000 genomes]
rs2127285	0.82[ASN][1000 genomes]
rs2199752	0.82[ASN][1000 genomes]
rs28883723	0.82[ASN][1000 genomes]
rs34946845	0.82[ASN][1000 genomes]
rs3921894	0.82[ASN][1000 genomes]
rs4336092	0.82[ASN][1000 genomes]
rs4336093	0.82[ASN][1000 genomes]
rs4583626	0.82[ASN][1000 genomes]
rs58745933	0.82[ASN][1000 genomes]
rs58977847	0.82[ASN][1000 genomes]
rs60181052	0.82[ASN][1000 genomes]
rs60457637	0.82[ASN][1000 genomes]
rs60752937	0.82[ASN][1000 genomes]
rs62272139	0.82[ASN][1000 genomes]
rs62272140	0.82[ASN][1000 genomes]
rs62272143	0.82[ASN][1000 genomes]
rs62272145	0.82[ASN][1000 genomes]
rs62272148	0.82[ASN][1000 genomes]
rs62274662	0.82[ASN][1000 genomes]
rs6441652	0.82[ASN][1000 genomes]
rs6441653	0.82[ASN][1000 genomes]
rs6441655	0.82[ASN][1000 genomes]
rs6441656	0.82[ASN][1000 genomes]
rs6762916	0.82[ASN][1000 genomes]
rs6767449	0.82[ASN][1000 genomes]
rs6773822	0.82[ASN][1000 genomes]
rs6779747	0.82[ASN][1000 genomes]
rs6779934	0.82[ASN][1000 genomes]
rs6796547	0.82[ASN][1000 genomes]
rs6799239	0.82[ASN][1000 genomes]
rs6799973	0.82[ASN][1000 genomes]
rs6808105	0.82[ASN][1000 genomes]
rs7611188	0.82[ASN][1000 genomes]
rs7611268	0.82[ASN][1000 genomes]
rs7618733	0.82[ASN][1000 genomes]
rs7623150	0.82[ASN][1000 genomes]
rs7625010	0.82[ASN][1000 genomes]
rs7628701	0.82[ASN][1000 genomes]
rs7633286	0.82[ASN][1000 genomes]
rs7635093	0.82[ASN][1000 genomes]
rs7637090	0.82[ASN][1000 genomes]
rs7644557	0.82[ASN][1000 genomes]
rs9816624	0.82[ASN][1000 genomes]
rs9824014	0.82[ASN][1000 genomes]
rs9832588	0.82[ASN][1000 genomes]
rs9832728	0.82[ASN][1000 genomes]
rs9838271	0.82[ASN][1000 genomes]
rs9838540	0.82[ASN][1000 genomes]
rs9846632	0.82[ASN][1000 genomes]
rs9855923	0.82[ASN][1000 genomes]
rs9856264	0.82[ASN][1000 genomes]
rs9860078	0.82[ASN][1000 genomes]
rs9869060	0.82[ASN][1000 genomes]
rs9869070	0.82[ASN][1000 genomes]
rs9875116	0.82[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	nsv497784	chr3:101315009-102092989	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	87 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:101968400-102016200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr3:101979800-101987800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr3:101982200-101983000	Weak transcription	Right Atrium	heart

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