Variant report

Variant	rs8094581
Chromosome Location	chr18:44818999-44819000
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs12326579	0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12605946	0.86[EUR][1000 genomes]
rs12608016	0.86[EUR][1000 genomes]
rs12608025	0.86[EUR][1000 genomes]
rs16950780	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs16951539	0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2082652	0.86[EUR][1000 genomes]
rs2082653	0.86[EUR][1000 genomes]
rs2684834	0.95[EUR][1000 genomes]
rs2850691	0.95[EUR][1000 genomes]
rs61645415	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7237929	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7239153	0.80[ASN][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	nsv833641	chr18:44815063-45020202	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA miRNA	2 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	chr18:44810400-44819200	Weak transcription	Muscle Satellite Cultured Cells	--

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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