Variant report

Variant	rs11919884
Chromosome Location	chr3:46301423-46301424
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 80 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs10510750	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11575062	0.84[EUR][1000 genomes]
rs13065351	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13068145	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13068271	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13071469	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13073976	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13077302	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13078564	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13080757	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13093063	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13096808	0.85[EUR][1000 genomes]
rs13100243	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17217831	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17283712	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17284138	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17284187	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1894387	0.84[EUR][1000 genomes]
rs1894388	0.84[EUR][1000 genomes]
rs28677778	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3091310	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3092957	0.84[EUR][1000 genomes]
rs3092958	0.84[EUR][1000 genomes]
rs3092959	0.84[EUR][1000 genomes]
rs34024447	0.84[EUR][1000 genomes]
rs34041956	0.84[EUR][1000 genomes]
rs34073838	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs34079287	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34106161	0.84[EUR][1000 genomes]
rs34180919	0.87[EUR][1000 genomes]
rs34272024	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34351442	0.87[EUR][1000 genomes]
rs34363105	0.84[EUR][1000 genomes]
rs34406035	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34448949	0.84[EUR][1000 genomes]
rs34473395	0.84[EUR][1000 genomes]
rs34578126	0.85[EUR][1000 genomes]
rs34709208	0.84[EUR][1000 genomes]
rs34988015	0.87[EUR][1000 genomes]
rs35035328	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35117954	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs35148665	0.87[EUR][1000 genomes]
rs35203745	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs35218998	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs35367413	0.84[EUR][1000 genomes]
rs35373513	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs35413141	0.84[EUR][1000 genomes]
rs35438577	0.84[EUR][1000 genomes]
rs35511592	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs35577626	0.87[EUR][1000 genomes]
rs35601704	0.84[EUR][1000 genomes]
rs35646896	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs35943069	0.80[EUR][1000 genomes]
rs36048333	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs36052732	0.84[EUR][1000 genomes]
rs36078103	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3749461	0.84[EUR][1000 genomes]
rs3918354	0.84[EUR][1000 genomes]
rs3918362	0.84[EUR][1000 genomes]
rs3918365	0.84[EUR][1000 genomes]
rs3918368	0.84[EUR][1000 genomes]
rs4473594	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4987053	0.81[AFR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6793370	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs71327047	0.88[EUR][1000 genomes]
rs71327048	0.87[EUR][1000 genomes]
rs71327052	0.81[EUR][1000 genomes]
rs71327053	0.82[EUR][1000 genomes]
rs71327054	0.84[EUR][1000 genomes]
rs71327055	0.84[EUR][1000 genomes]
rs71327056	0.84[EUR][1000 genomes]
rs71327057	0.84[EUR][1000 genomes]
rs71615445	0.84[EUR][1000 genomes]
rs71622511	0.86[AFR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7649905	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9810242	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9872023	0.88[EUR][1000 genomes]
rs9882616	0.88[EUR][1000 genomes];0.84[ASN][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	nsv876734	chr3:45725031-46468467	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv498008	chr3:45733423-46319401	Strong transcription Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 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	chr3:46300600-46303200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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