Variant report

Variant	rs72767603
Chromosome Location	chr5:97367720-97367721
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs2352234	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4482923	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56326964	1.00[EUR][1000 genomes]
rs58956624	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60418505	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61327763	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72767617	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72767619	1.00[AMR][1000 genomes]
rs72767623	1.00[AMR][1000 genomes]
rs72767624	1.00[AMR][1000 genomes]
rs72767625	1.00[AMR][1000 genomes]
rs72767635	1.00[AMR][1000 genomes]
rs72767636	1.00[AMR][1000 genomes]
rs72767638	1.00[AMR][1000 genomes]
rs72767640	1.00[AMR][1000 genomes]
rs72767644	1.00[AMR][1000 genomes]
rs72767646	1.00[AMR][1000 genomes]
rs72767648	1.00[AMR][1000 genomes]
rs72767649	1.00[AMR][1000 genomes]
rs72767650	1.00[AMR][1000 genomes]
rs72767651	1.00[AMR][1000 genomes]
rs72767655	1.00[AMR][1000 genomes]
rs72767657	1.00[AMR][1000 genomes]
rs72769642	1.00[AMR][1000 genomes]
rs72783504	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72783506	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72783508	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72783510	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72783522	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72783524	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72783526	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72783527	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72783528	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72783541	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72783543	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72783544	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72783545	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72783546	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72783547	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72783549	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72783554	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72783556	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72783557	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72783559	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72783561	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016231	chr5:97206242-97420435	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1021856	chr5:97258323-97414178	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv599062	chr5:97258619-97430527	Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv2830155	chr5:97278902-97425123	Active TSS Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv882404	chr5:97281641-97638743	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv1031989	chr5:97333291-97524353	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1034472	chr5:97357264-97523965	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr5:97367000-97368600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr5:97367200-97368000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr5:97367200-97368000	Enhancers	NHEK	skin
4	chr5:97367400-97367800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr5:97367400-97368000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr5:97367600-97368200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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