Variant report

Variant	rs10163633
Chromosome Location	chr18:44818151-44818152
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10164040	0.81[EUR][1000 genomes]
rs11082575	0.92[CEU][hapmap]
rs12327454	0.82[EUR][1000 genomes]
rs12607072	0.85[EUR][1000 genomes]
rs12960592	0.83[EUR][1000 genomes]
rs12960952	0.83[EUR][1000 genomes]
rs1347340	0.90[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs1347343	0.88[EUR][1000 genomes]
rs1434518	0.87[EUR][1000 genomes]
rs16950733	0.95[ASN][1000 genomes]
rs1893787	0.83[EUR][1000 genomes]
rs28391188	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28417368	0.95[ASN][1000 genomes]
rs28650321	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4452038	0.83[EUR][1000 genomes]
rs7240132	0.83[EUR][1000 genomes]
rs919979	0.93[CEU][hapmap]

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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