Variant report

Variant	rs59946294
Chromosome Location	chr21:29013300-29013301
allele	A/C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs11088038	0.87[EUR][1000 genomes]
rs11701315	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11702066	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12482624	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12483350	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12483741	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16980990	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2156296	0.83[EUR][1000 genomes]
rs2831033	0.87[EUR][1000 genomes]
rs2831041	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2831042	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2831043	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2831044	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2831045	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2831048	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2831049	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2831050	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2831053	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4817183	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7275935	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7278716	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73382076	0.87[EUR][1000 genomes]
rs73384054	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73384056	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73384059	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73384066	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73384078	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73384086	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs73386055	0.88[EUR][1000 genomes]
rs928273	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9636797	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1067475	chr21:28238746-29046707	Enhancers Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv459229	chr21:28543456-29482488	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv587342	chr21:28543456-29482488	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
4	nsv1059423	chr21:28957144-29306656	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:28970400-29018000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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