Variant report

Variant	rs34094616
Chromosome Location	chr14:79876361-79876362
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:79875683..79878645-chr5:173629859..173632851,2	MCF-7	breast:

Extended variants
information (count: 38 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10450934	0.87[AMR][1000 genomes]
rs10450935	0.88[AMR][1000 genomes]
rs10873322	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11159408	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11622878	0.84[AMR][1000 genomes]
rs11625634	0.88[AMR][1000 genomes]
rs12888219	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12888940	0.88[AMR][1000 genomes]
rs17758133	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1984716	0.88[AMR][1000 genomes]
rs1993009	0.88[AMR][1000 genomes]
rs1993011	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1993012	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2164434	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2164435	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2196444	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2196446	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2217887	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2218782	0.87[AMR][1000 genomes]
rs2574750	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2574751	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2574752	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2597086	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2597087	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2597089	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2597091	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2597092	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34848585	0.99[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35820490	0.88[AMR][1000 genomes]
rs61993113	0.99[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61993118	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs714276	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs954860	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	nsv902110	chr14:79624492-79998294	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv530072	chr14:79769657-79928269	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv902111	chr14:79807197-79890677	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3429119	chr14:79874849-79877397	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79867800-79877600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr14:79872600-79884800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr14:79874200-79877800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr14:79874400-79877200	Weak transcription	NHEK	skin
5	chr14:79874600-79877600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr14:79874600-79878200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr14:79875600-79880000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr14:79875800-79879800	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr14:79875800-79879800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr14:79875800-79880200	Weak transcription	HUES48 Cell Line	embryonic stem cell

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