Variant report

Variant	rs73875968
Chromosome Location	chr3:161689105-161689106
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs58454904	1.00[AMR][1000 genomes]
rs59116586	1.00[AMR][1000 genomes]
rs6772107	1.00[AMR][1000 genomes]
rs73875903	1.00[AMR][1000 genomes]
rs73875907	1.00[AMR][1000 genomes]
rs73875922	1.00[AMR][1000 genomes]
rs73875941	1.00[AMR][1000 genomes]
rs73875960	1.00[AMR][1000 genomes]
rs73875961	1.00[AMR][1000 genomes]
rs73875969	1.00[AMR][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	nsv533237	chr3:161019834-161804660	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	91 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:161688200-161693200	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr3:161688600-161690600	Weak transcription	Fetal Heart	heart

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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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