Variant report

Variant	rs34762534
Chromosome Location	chr5:52693173-52693174
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs10940312	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10940315	0.83[ASN][1000 genomes]
rs10940316	0.83[ASN][1000 genomes]
rs11740573	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11741680	0.83[ASN][1000 genomes]
rs11741921	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11742633	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11745102	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11745979	0.83[ASN][1000 genomes]
rs11746509	0.83[ASN][1000 genomes]
rs11746732	0.83[ASN][1000 genomes]
rs11748797	0.83[ASN][1000 genomes]
rs11748901	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11955043	0.83[ASN][1000 genomes]
rs12153178	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12153379	0.82[ASN][1000 genomes]
rs12153556	0.93[ASN][1000 genomes]
rs13153643	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13157909	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13161996	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13162472	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13163361	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13170709	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13171352	0.83[ASN][1000 genomes]
rs13171813	0.83[ASN][1000 genomes]
rs13175475	0.83[ASN][1000 genomes]
rs13176460	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13179666	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13183277	0.83[ASN][1000 genomes]
rs13188654	0.81[ASN][1000 genomes]
rs13188772	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1363971	0.81[ASN][1000 genomes]
rs1423549	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1423559	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1423561	0.82[ASN][1000 genomes]
rs1469100	0.82[ASN][1000 genomes]
rs2042331	0.81[ASN][1000 genomes]
rs34256928	0.83[ASN][1000 genomes]
rs34274925	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34483113	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34492969	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34547502	0.85[ASN][1000 genomes]
rs34690366	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34801686	0.83[ASN][1000 genomes]
rs34942708	0.83[ASN][1000 genomes]
rs34985749	0.84[ASN][1000 genomes]
rs35201567	0.83[ASN][1000 genomes]
rs35237162	0.83[ASN][1000 genomes]
rs35257227	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35586638	0.83[ASN][1000 genomes]
rs35930552	0.83[ASN][1000 genomes]
rs36125518	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3943929	0.82[ASN][1000 genomes]
rs4131065	0.83[ASN][1000 genomes]
rs4254863	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4254864	0.83[ASN][1000 genomes]
rs4274942	0.83[ASN][1000 genomes]
rs4279297	0.85[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs4301187	0.83[ASN][1000 genomes]
rs4499786	0.83[ASN][1000 genomes]
rs4535418	0.83[ASN][1000 genomes]
rs4568325	0.83[ASN][1000 genomes]
rs55880944	0.83[ASN][1000 genomes]
rs62357829	0.83[ASN][1000 genomes]
rs62357837	0.83[ASN][1000 genomes]
rs62357857	0.83[ASN][1000 genomes]
rs62357858	0.83[ASN][1000 genomes]
rs62357859	0.81[ASN][1000 genomes]
rs62359260	0.81[ASN][1000 genomes]
rs62359263	0.83[ASN][1000 genomes]
rs71592629	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs71619953	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][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	nsv949005	chr5:52188028-52808229	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	esv2752745	chr5:52422063-53343529	Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv830297	chr5:52492494-52707758	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv508356	chr5:52646168-52703120	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1032632	chr5:52667145-53655624	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:52689200-52693200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:52692400-52696400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr5:52692600-52693200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr5:52692600-52697200	Enhancers	NHDF-Ad	bronchial
5	chr5:52692800-52694200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr5:52692800-52695200	Enhancers	Hela-S3	cervix
7	chr5:52692800-52696400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr5:52692800-52697200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr5:52693000-52694000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr5:52693000-52694400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr5:52693000-52694400	Enhancers	HMEC	breast
12	chr5:52693000-52694600	Enhancers	HSMM	muscle
13	chr5:52693000-52696600	Enhancers	NHLF	lung

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