Variant report

Variant	rs73316615
Chromosome Location	chr14:79503108-79503109
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10129622	1.00[AMR][1000 genomes]
rs10129767	1.00[AMR][1000 genomes]
rs10130794	0.84[AFR][1000 genomes]
rs10131285	0.84[AFR][1000 genomes]
rs10132523	1.00[AMR][1000 genomes]
rs10134044	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10134881	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10136667	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10137034	0.84[AFR][1000 genomes]
rs10140005	0.83[AFR][1000 genomes]
rs10141967	0.90[AFR][1000 genomes]
rs10143938	1.00[AMR][1000 genomes]
rs10144702	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10150043	1.00[AMR][1000 genomes]
rs10150236	1.00[AMR][1000 genomes]
rs10150326	1.00[AMR][1000 genomes]
rs10150906	0.86[AFR][1000 genomes]
rs10151063	1.00[AMR][1000 genomes]
rs10438175	1.00[AMR][1000 genomes]
rs13379131	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13379188	0.87[AFR][1000 genomes]
rs13379304	0.84[AFR][1000 genomes]
rs2062743	0.82[AFR][1000 genomes]
rs28376793	0.83[AFR][1000 genomes]
rs28547245	0.87[AFR][1000 genomes]
rs28667554	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28673990	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4609770	0.83[AFR][1000 genomes]
rs60089514	1.00[AMR][1000 genomes]
rs60147420	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60958288	0.83[AFR][1000 genomes]
rs7141297	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73316627	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73317278	1.00[AMR][1000 genomes]
rs73317280	1.00[AMR][1000 genomes]
rs73318802	1.00[AMR][1000 genomes]
rs73320815	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73322876	0.90[AFR][1000 genomes]
rs73322893	0.83[AFR][1000 genomes]
rs73324705	0.88[AFR][1000 genomes]
rs73324730	0.83[AFR][1000 genomes]
rs73324740	0.87[AFR][1000 genomes]
rs73324748	0.83[AFR][1000 genomes]
rs73332955	1.00[AMR][1000 genomes]
rs8014991	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 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	nsv1037112	chr14:79412455-79527656	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	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
5	nsv1046464	chr14:79478352-79514789	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	lncRNA	n/a	inside rSNPs	diseases
6	nsv1036542	chr14:79478352-79518230	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	lncRNA	n/a	inside rSNPs	diseases
7	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

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79495200-79506400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr14:79502200-79504400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr14:79502600-79503400	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr14:79502800-79503200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr14:79503000-79503800	Enhancers	Primary monocytes fromperipheralblood	blood

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