Variant report

Variant	rs4294366
Chromosome Location	chr1:47355491-47355492
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs11803288	0.90[AMR][1000 genomes]
rs12062956	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12064597	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12068907	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12075287	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12082613	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17102905	1.00[AMR][1000 genomes]
rs45584834	0.90[AMR][1000 genomes]
rs4646476	1.00[JPT][hapmap]
rs4646488	1.00[JPT][hapmap]
rs4646494	1.00[JPT][hapmap]
rs4646496	1.00[JPT][hapmap]
rs56839286	1.00[AMR][1000 genomes]
rs57007364	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs57190303	1.00[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs57282306	0.90[AMR][1000 genomes]
rs57557506	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs57627915	1.00[AMR][1000 genomes]
rs58223210	1.00[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs58307605	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58422947	1.00[AMR][1000 genomes]
rs58688699	1.00[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs59402146	0.90[AMR][1000 genomes]
rs59465754	1.00[ASN][1000 genomes]
rs59903483	1.00[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs60189155	1.00[AMR][1000 genomes]
rs60952216	1.00[AMR][1000 genomes]
rs61449393	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7526965	1.00[AMR][1000 genomes]
rs7556308	1.00[AMR][1000 genomes]
rs9333003	1.00[AMR][1000 genomes]
rs9333007	1.00[AMR][1000 genomes]
rs9333032	1.00[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs9333037	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1013048	chr1:47132831-47377364	Genic enhancers Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv534955	chr1:47132831-47377364	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv871958	chr1:47350374-47517123	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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