Variant report

Variant	rs73459467
Chromosome Location	chr7:147181828-147181829
allele	C/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]
rs58307467	1.00[AMR][1000 genomes]
rs6967847	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73457452	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73459461	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73459464	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73475120	1.00[AMR][1000 genomes]
rs73475122	1.00[AMR][1000 genomes]
rs73475124	1.00[AMR][1000 genomes]
rs73475134	1.00[AMR][1000 genomes]
rs73475137	0.88[AFR][1000 genomes];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	nsv931005	chr7:146730472-147381257	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 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	chr7:147180600-147183200	Enhancers	Muscle Satellite Cultured Cells	--
2	chr7:147180800-147182200	Enhancers	Osteobl	bone

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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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