Variant report

Variant	rs9496046
Chromosome Location	chr6:141817745-141817746
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10080954	0.94[AFR][1000 genomes]
rs10223657	1.00[AMR][1000 genomes]
rs58606500	0.94[AFR][1000 genomes]
rs58761168	1.00[AMR][1000 genomes]
rs6901804	1.00[AMR][1000 genomes]
rs6933512	1.00[AMR][1000 genomes]
rs6933872	1.00[AMR][1000 genomes]
rs7759070	1.00[AMR][1000 genomes]
rs9484513	0.94[AFR][1000 genomes]
rs9484515	1.00[AMR][1000 genomes]
rs9484524	1.00[AMR][1000 genomes]
rs9484526	1.00[AMR][1000 genomes]
rs9496034	0.83[AFR][1000 genomes]
rs9496035	0.94[AFR][1000 genomes]
rs9496036	0.94[AFR][1000 genomes]
rs9496038	0.94[AFR][1000 genomes]
rs9496039	0.94[AFR][1000 genomes]
rs9496040	0.94[AFR][1000 genomes]
rs9496041	0.94[AFR][1000 genomes]
rs9496042	0.94[AFR][1000 genomes]
rs9496043	0.88[AFR][1000 genomes]
rs9496047	1.00[AMR][1000 genomes]
rs9496048	1.00[AMR][1000 genomes]
rs9496051	1.00[AMR][1000 genomes]
rs9496052	1.00[AMR][1000 genomes]
rs9496060	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019459	chr6:141051249-141862727	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv538453	chr6:141051249-141862727	ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv532070	chr6:141057326-141865359	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1025922	chr6:141090901-141865360	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv538454	chr6:141090901-141865360	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv1029550	chr6:141372610-142029669	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv1015835	chr6:141713451-142233317	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	nsv538455	chr6:141713451-142233317	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	esv2755719	chr6:141721907-142123546	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:141806200-141827600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:141814400-141824400	Weak transcription	Aorta	Aorta
3	chr6:141816000-141817800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr6:141817400-141818200	Enhancers	Primary B cells from peripheral blood	blood
5	chr6:141817600-141818000	Enhancers	Primary B cells from cord blood	blood
6	chr6:141817600-141818200	Enhancers	Dnd41	blood

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