Variant report

Variant	rs4692123
Chromosome Location	chr4:26536095-26536096
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10015526	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10939120	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11933322	1.00[ASN][1000 genomes]
rs12054535	1.00[ASN][1000 genomes]
rs12511054	0.84[AFR][1000 genomes]
rs12648115	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1387542	0.91[AFR][1000 genomes]
rs166353	0.85[JPT][hapmap]
rs16878454	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16878474	1.00[ASN][1000 genomes]
rs2007586	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2171750	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28678865	0.96[ASN][1000 genomes]
rs3899075	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4572860	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4692122	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4692125	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4692547	1.00[ASN][1000 genomes]
rs6821178	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6822462	1.00[ASN][1000 genomes]
rs6838579	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6838762	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6856499	1.00[ASN][1000 genomes]
rs73112763	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73810755	1.00[ASN][1000 genomes]
rs73810790	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73810792	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73810793	1.00[ASN][1000 genomes]
rs73810795	1.00[ASN][1000 genomes]
rs73810797	1.00[ASN][1000 genomes]
rs970730	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs970731	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[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	esv2762417	chr4:26491768-26576800	Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	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	chr4:26532200-26536600	Weak transcription	HSMMtube	muscle

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