Variant report

Variant	rs11640447
Chromosome Location	chr16:80017582-80017583
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:80004622..80006515-chr16:80014289..80017872,4	K562	blood:

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs10514477	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11640073	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16951797	0.82[EUR][1000 genomes]
rs16951799	0.84[EUR][1000 genomes]
rs16951801	0.84[EUR][1000 genomes]
rs16951803	0.82[EUR][1000 genomes]
rs16951814	0.84[EUR][1000 genomes]
rs16951838	0.84[EUR][1000 genomes]
rs16951842	0.84[EUR][1000 genomes]
rs16951843	0.84[EUR][1000 genomes]
rs16951873	0.87[EUR][1000 genomes]
rs16951897	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs16951906	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs34819814	0.84[EUR][1000 genomes]
rs4243193	0.84[EUR][1000 genomes]
rs4243195	0.84[EUR][1000 genomes]
rs4300657	0.84[EUR][1000 genomes]
rs4337307	0.84[EUR][1000 genomes]
rs4337308	0.84[EUR][1000 genomes]
rs4344762	0.84[EUR][1000 genomes]
rs4371170	0.84[EUR][1000 genomes]
rs4398121	0.84[EUR][1000 genomes]
rs4429310	0.84[EUR][1000 genomes]
rs4430760	0.84[EUR][1000 genomes]
rs4473201	0.87[EUR][1000 genomes]
rs4474699	0.87[EUR][1000 genomes]
rs4591155	0.84[EUR][1000 genomes]
rs4600478	0.84[EUR][1000 genomes]
rs4600479	0.84[EUR][1000 genomes]
rs4613081	0.84[EUR][1000 genomes]
rs4643335	0.84[EUR][1000 genomes]
rs4889058	0.80[EUR][1000 genomes]
rs4889060	0.84[EUR][1000 genomes]
rs4889063	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs58399708	0.83[EUR][1000 genomes]
rs62040147	0.84[EUR][1000 genomes]
rs62040149	0.83[EUR][1000 genomes]
rs62040150	0.83[EUR][1000 genomes]
rs62040151	0.84[EUR][1000 genomes]
rs62040152	0.84[EUR][1000 genomes]
rs62040153	0.84[EUR][1000 genomes]
rs62040154	0.84[EUR][1000 genomes]
rs62040155	0.84[EUR][1000 genomes]
rs62040157	0.84[EUR][1000 genomes]
rs62040158	0.84[EUR][1000 genomes]
rs62040159	0.84[EUR][1000 genomes]
rs62042260	0.84[EUR][1000 genomes]
rs62042261	0.84[EUR][1000 genomes]
rs62042262	0.84[EUR][1000 genomes]
rs62042264	0.87[EUR][1000 genomes]
rs62042286	0.87[EUR][1000 genomes]
rs62042287	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs62042288	0.87[EUR][1000 genomes]
rs62042290	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62042291	0.87[EUR][1000 genomes]
rs62042292	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs62042293	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62042294	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62042295	0.87[EUR][1000 genomes]
rs62042296	0.86[EUR][1000 genomes]
rs62042298	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62042299	0.97[EUR][1000 genomes]
rs62042300	0.97[EUR][1000 genomes]
rs62042301	0.97[EUR][1000 genomes]
rs62042302	0.97[EUR][1000 genomes]
rs62042304	0.91[EUR][1000 genomes]
rs62042323	0.94[EUR][1000 genomes]
rs7190101	0.91[EUR][1000 genomes]
rs7192124	0.91[EUR][1000 genomes]
rs7195573	0.97[EUR][1000 genomes]
rs7204058	0.84[EUR][1000 genomes]
rs7204532	0.84[EUR][1000 genomes]
rs74038404	0.84[EUR][1000 genomes]
rs8044242	0.87[EUR][1000 genomes]
rs8044773	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8053286	0.85[EUR][1000 genomes]
rs9319546	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9788812	0.96[EUR][1000 genomes]
rs9788879	0.97[EUR][1000 genomes]
rs9788937	0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 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
3	esv3360836	chr16:80013751-80018049	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:80015400-80020000	Weak transcription	HMEC	breast

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