Variant report

Variant	rs62392264
Chromosome Location	chr5:145015941-145015942
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10036303	0.89[EUR][1000 genomes]
rs10040900	0.89[EUR][1000 genomes]
rs10041019	0.89[EUR][1000 genomes]
rs10043918	0.89[EUR][1000 genomes]
rs10046079	0.89[EUR][1000 genomes]
rs10059454	0.89[EUR][1000 genomes]
rs10061046	0.89[EUR][1000 genomes]
rs10064838	0.89[EUR][1000 genomes]
rs10069261	0.95[EUR][1000 genomes]
rs10072272	0.89[EUR][1000 genomes]
rs10477282	0.89[EUR][1000 genomes]
rs11951086	0.89[EUR][1000 genomes]
rs13355336	0.89[EUR][1000 genomes]
rs13356922	0.89[EUR][1000 genomes]
rs13360440	0.89[EUR][1000 genomes]
rs1363554	0.95[EUR][1000 genomes]
rs1835976	0.89[EUR][1000 genomes]
rs28377159	0.95[EUR][1000 genomes]
rs28490156	0.95[EUR][1000 genomes]
rs28536780	0.95[EUR][1000 genomes]
rs28584959	0.95[EUR][1000 genomes]
rs28604887	0.89[EUR][1000 genomes]
rs28715852	0.95[EUR][1000 genomes]
rs28814957	0.89[EUR][1000 genomes]
rs57049514	0.95[EUR][1000 genomes]
rs58980830	0.89[EUR][1000 genomes]
rs61316690	0.89[EUR][1000 genomes]
rs62392265	0.95[EUR][1000 genomes]
rs62392285	0.84[EUR][1000 genomes]
rs62392706	0.89[EUR][1000 genomes]
rs62392709	0.95[EUR][1000 genomes]
rs62392711	0.95[EUR][1000 genomes]
rs62392716	0.95[EUR][1000 genomes]
rs62394187	0.95[EUR][1000 genomes]
rs62394189	0.95[EUR][1000 genomes]
rs62394212	0.95[EUR][1000 genomes]
rs62394214	0.95[EUR][1000 genomes]
rs62394218	0.95[EUR][1000 genomes]
rs62394220	0.95[EUR][1000 genomes]
rs62394221	0.95[EUR][1000 genomes]
rs62394223	0.95[EUR][1000 genomes]
rs62395867	0.89[EUR][1000 genomes]
rs6874465	0.89[EUR][1000 genomes]
rs6884965	0.89[EUR][1000 genomes]
rs73311508	0.89[EUR][1000 genomes]
rs9968717	0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv883004	chr5:144945649-145068001	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv883005	chr5:144945649-145107586	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	Chromatin interactive region lncRNA	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	chr5:145015200-145016200	Enhancers	Placenta Amnion	Placenta Amnion

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