Variant report

Variant	rs62042298
Chromosome Location	chr16:80019628-80019629
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs10514477	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11640073	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11640447	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16951799	0.82[EUR][1000 genomes]
rs16951801	0.82[EUR][1000 genomes]
rs16951814	0.82[EUR][1000 genomes]
rs16951838	0.82[EUR][1000 genomes]
rs16951842	0.82[EUR][1000 genomes]
rs16951843	0.82[EUR][1000 genomes]
rs16951873	0.84[EUR][1000 genomes]
rs16951897	0.84[EUR][1000 genomes]
rs16951906	0.84[EUR][1000 genomes]
rs34819814	0.82[EUR][1000 genomes]
rs4243193	0.82[EUR][1000 genomes]
rs4243195	0.82[EUR][1000 genomes]
rs4300657	0.82[EUR][1000 genomes]
rs4337307	0.82[EUR][1000 genomes]
rs4337308	0.82[EUR][1000 genomes]
rs4344762	0.82[EUR][1000 genomes]
rs4371170	0.82[EUR][1000 genomes]
rs4398121	0.82[EUR][1000 genomes]
rs4429310	0.82[EUR][1000 genomes]
rs4430760	0.82[EUR][1000 genomes]
rs4473201	0.84[EUR][1000 genomes]
rs4474699	0.84[EUR][1000 genomes]
rs4591155	0.82[EUR][1000 genomes]
rs4600478	0.82[EUR][1000 genomes]
rs4600479	0.82[EUR][1000 genomes]
rs4613081	0.82[EUR][1000 genomes]
rs4643335	0.82[EUR][1000 genomes]
rs4889060	0.82[EUR][1000 genomes]
rs4889063	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58399708	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62040147	0.82[EUR][1000 genomes]
rs62040149	0.80[EUR][1000 genomes]
rs62040150	0.80[EUR][1000 genomes]
rs62040151	0.82[EUR][1000 genomes]
rs62040152	0.82[EUR][1000 genomes]
rs62040153	0.82[EUR][1000 genomes]
rs62040154	0.82[EUR][1000 genomes]
rs62040155	0.82[EUR][1000 genomes]
rs62040157	0.82[EUR][1000 genomes]
rs62040158	0.82[EUR][1000 genomes]
rs62040159	0.82[EUR][1000 genomes]
rs62042260	0.82[EUR][1000 genomes]
rs62042261	0.82[EUR][1000 genomes]
rs62042262	0.82[EUR][1000 genomes]
rs62042264	0.84[EUR][1000 genomes]
rs62042286	0.84[EUR][1000 genomes]
rs62042287	0.84[EUR][1000 genomes]
rs62042288	0.84[EUR][1000 genomes]
rs62042290	0.82[EUR][1000 genomes]
rs62042291	0.84[EUR][1000 genomes]
rs62042292	0.82[EUR][1000 genomes]
rs62042293	0.84[EUR][1000 genomes]
rs62042294	0.84[EUR][1000 genomes]
rs62042295	0.84[EUR][1000 genomes]
rs62042296	0.83[EUR][1000 genomes]
rs62042299	1.00[EUR][1000 genomes]
rs62042300	1.00[EUR][1000 genomes]
rs62042301	1.00[EUR][1000 genomes]
rs62042302	1.00[EUR][1000 genomes]
rs62042304	0.94[EUR][1000 genomes]
rs62042323	0.97[EUR][1000 genomes]
rs7190101	0.94[EUR][1000 genomes]
rs7192124	0.94[EUR][1000 genomes]
rs7195573	1.00[EUR][1000 genomes]
rs7204058	0.82[EUR][1000 genomes]
rs7204532	0.82[EUR][1000 genomes]
rs74038404	0.82[EUR][1000 genomes]
rs8044242	0.84[EUR][1000 genomes]
rs8044773	0.84[EUR][1000 genomes]
rs8053286	0.87[EUR][1000 genomes]
rs9319546	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9788812	0.99[EUR][1000 genomes]
rs9788879	1.00[EUR][1000 genomes]
rs9788937	0.94[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	nsv573285	chr16:79158182-80127326	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv573294	chr16:80005642-80131944	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:80015400-80020000	Weak transcription	HMEC	breast
2	chr16:80018600-80019800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr16:80019600-80020600	Enhancers	Fetal Lung	lung

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