Variant report

Variant	rs4382439
Chromosome Location	chr8:39071297-39071298
allele	C/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:34)

rs_ID	r²[population]
rs12680934	0.87[AFR][1000 genomes]
rs4288342	1.00[AMR][1000 genomes]
rs4398876	0.99[AFR][1000 genomes]
rs4404879	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4416797	0.99[AFR][1000 genomes]
rs4476978	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4481554	0.93[AFR][1000 genomes]
rs4537269	0.96[AFR][1000 genomes]
rs4590406	0.94[AFR][1000 genomes]
rs4636164	0.87[AFR][1000 genomes]
rs4733906	0.87[AFR][1000 genomes]
rs4733984	0.87[AFR][1000 genomes]
rs59851050	1.00[AMR][1000 genomes]
rs60402210	1.00[AMR][1000 genomes]
rs6474122	0.96[AFR][1000 genomes]
rs6983342	1.00[AMR][1000 genomes]
rs6984156	1.00[AMR][1000 genomes]
rs6987728	1.00[AMR][1000 genomes]
rs6988368	0.99[AFR][1000 genomes]
rs6999436	1.00[AMR][1000 genomes]
rs7000417	1.00[AMR][1000 genomes]
rs7001987	1.00[AMR][1000 genomes]
rs7003066	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7013465	1.00[AMR][1000 genomes]
rs7816599	1.00[AMR][1000 genomes]
rs7817462	1.00[AMR][1000 genomes]
rs7822099	1.00[AMR][1000 genomes]
rs7823183	0.87[AFR][1000 genomes]
rs7831826	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7833198	1.00[AMR][1000 genomes]
rs7840897	1.00[AMR][1000 genomes]
rs7844092	1.00[AMR][1000 genomes]
rs7844395	1.00[AMR][1000 genomes]
rs7845771	0.96[AFR][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	nsv1015907	chr8:38967169-39718559	Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv539550	chr8:38967169-39718559	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv1027443	chr8:38993423-39181079	Strong transcription ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv539551	chr8:38993423-39181079	Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv428198	chr8:39069309-39405724	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr8:39060400-39082600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr8:39064600-39075800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:39067800-39075800	Weak transcription	Ovary	ovary

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