Variant report

Variant	rs62291005
Chromosome Location	chr3:180200822-180200823
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs1353679	0.90[EUR][1000 genomes]
rs1532485	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1603658	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17707963	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17708913	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17764356	0.82[EUR][1000 genomes]
rs28385473	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs28495789	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62291004	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62291006	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62291007	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62291008	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62291009	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62291043	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62291045	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62291048	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6770664	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6774942	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7626274	0.81[EUR][1000 genomes]
rs9290705	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9819839	0.92[EUR][1000 genomes]
rs9837678	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9846858	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9847201	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9857489	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9858483	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9864959	0.92[EUR][1000 genomes]
rs9866580	0.92[EUR][1000 genomes]
rs9872076	0.92[EUR][1000 genomes]
rs9876153	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9877497	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012271	chr3:179806875-180234871	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1007831	chr3:180162003-180348203	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv536818	chr3:180162003-180348203	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr3:180187400-180205600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr3:180200000-180201400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr3:180200000-180208400	Weak transcription	HMEC	breast

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