Variant report

Variant	rs73847071
Chromosome Location	chr3:94631657-94631658
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs1579543	1.00[AMR][1000 genomes]
rs57431896	1.00[AMR][1000 genomes]
rs58014210	1.00[AMR][1000 genomes]
rs58086527	1.00[AMR][1000 genomes]
rs58204392	1.00[AMR][1000 genomes]
rs59975236	1.00[AMR][1000 genomes]
rs60472824	1.00[AMR][1000 genomes]
rs73847062	1.00[AMR][1000 genomes]
rs73847076	1.00[AMR][1000 genomes]
rs73847077	1.00[AMR][1000 genomes]
rs73847080	1.00[AMR][1000 genomes]
rs73847085	1.00[AMR][1000 genomes]
rs73847088	1.00[AMR][1000 genomes]
rs73847092	1.00[AMR][1000 genomes]
rs73847093	1.00[AMR][1000 genomes]
rs73848726	1.00[AMR][1000 genomes]
rs73848727	1.00[AMR][1000 genomes]
rs73848734	1.00[AMR][1000 genomes]
rs973259	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv460764	chr3:94479849-94654181	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv590989	chr3:94479849-94654181	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 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	chr3:94630800-94632600	Enhancers	Hela-S3	cervix

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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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