Variant report

Variant	rs73322876
Chromosome Location	chr14:79542037-79542038
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10130794	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10131285	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10134044	0.82[AFR][1000 genomes]
rs10137034	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10140005	0.82[AFR][1000 genomes]
rs10141967	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10144702	0.83[AFR][1000 genomes]
rs10149302	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10150122	1.00[AMR][1000 genomes]
rs10150906	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13379131	0.87[AFR][1000 genomes]
rs13379188	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13379304	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28376793	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28450317	1.00[AMR][1000 genomes]
rs28547245	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28667554	0.90[AFR][1000 genomes]
rs28673990	0.86[AFR][1000 genomes]
rs4609770	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59058794	1.00[AMR][1000 genomes]
rs60147420	0.90[AFR][1000 genomes]
rs60958288	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7142699	1.00[AMR][1000 genomes]
rs73316615	0.90[AFR][1000 genomes]
rs73316627	0.83[AFR][1000 genomes]
rs73320815	0.87[AFR][1000 genomes]
rs73322893	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73324705	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73324730	0.93[AFR][1000 genomes]
rs73324740	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73324748	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73325827	1.00[AMR][1000 genomes]
rs8014991	0.94[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917249	chr14:79388181-79574717	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv1041991	chr14:79394408-79644886	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv931412	chr14:79420297-79928269	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv948724	chr14:79484233-79614043	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv565247	chr14:79508316-79555651	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	esv2761846	chr14:79522198-79629157	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79540800-79543800	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr14:79541200-79543200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr14:79541800-79542800	Enhancers	Pancreas	Pancrea
4	chr14:79541800-79543200	Enhancers	Colon Smooth Muscle	Colon

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