Variant report

Variant	rs73123446
Chromosome Location	chr3:84246435-84246436
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10212311	0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs13316720	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13353445	0.92[AFR][1000 genomes]
rs28373681	0.93[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs28616698	0.98[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28767329	0.92[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs35678260	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs4276195	0.95[ASN][1000 genomes]
rs55807627	0.93[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs55857229	0.93[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs56133340	0.83[AFR][1000 genomes]
rs66499339	0.92[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs66699133	0.92[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs67122732	0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs67502383	0.92[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6764253	0.95[ASN][1000 genomes]
rs6774268	0.93[ASN][1000 genomes]
rs68097135	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs73121758	0.83[AFR][1000 genomes]
rs73121759	0.83[AFR][1000 genomes]
rs73121799	0.93[AFR][1000 genomes]
rs9810168	0.95[ASN][1000 genomes]
rs9837479	0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9837793	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs9849196	0.93[AFR][1000 genomes]
rs9851115	0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9855231	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9857309	1.00[ASN][1000 genomes]
rs9858116	0.92[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs9861365	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9867026	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9867339	0.98[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9868702	0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9875009	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9985384	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	nsv1006081	chr3:83421626-84262106	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1007008	chr3:84069044-84653896	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv536612	chr3:84069044-84653896	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv460743	chr3:84094818-84644186	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv590814	chr3:84094818-84644186	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv590848	chr3:84200533-84560784	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	esv2760745	chr3:84208364-84783259	Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv1012551	chr3:84235733-84550197	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv536613	chr3:84235733-84550197	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:84215200-84248000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr3:84245800-84246600	ZNF genes & repeats	Adipose Nuclei	Adipose
3	chr3:84246000-84246800	ZNF genes & repeats	Pancreas	Pancrea

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