Variant report

Variant	rs73328860
Chromosome Location	chr8:122879389-122879390
allele	A/G
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]
rs10110191	0.83[AMR][1000 genomes]
rs10112095	0.83[AMR][1000 genomes]
rs16896151	0.83[AMR][1000 genomes]
rs16896176	0.83[AMR][1000 genomes]
rs16896185	0.83[AMR][1000 genomes]
rs73326803	0.83[AMR][1000 genomes]
rs73326826	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7814424	0.83[AMR][1000 genomes]
rs7844994	0.83[AMR][1000 genomes]
rs9297654	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	esv2752207	chr8:122869651-122961848	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:122870600-122881800	Weak transcription	NHDF-Ad	bronchial

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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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