Variant report

Variant	rs72739211
Chromosome Location	chr5:27159514-27159515
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs4259141	0.85[ASN][1000 genomes]
rs4331861	0.91[EUR][1000 genomes]
rs4382124	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4392592	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4429812	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4429813	0.91[EUR][1000 genomes]
rs4487458	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4496679	0.92[EUR][1000 genomes]
rs4518345	0.92[EUR][1000 genomes]
rs4555745	0.85[ASN][1000 genomes]
rs4597930	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4604162	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4604163	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4640754	0.91[EUR][1000 genomes]
rs56954447	0.91[EUR][1000 genomes]
rs61673971	0.90[EUR][1000 genomes]
rs66712717	0.90[ASN][1000 genomes]
rs72740668	0.91[EUR][1000 genomes]
rs72740669	0.91[EUR][1000 genomes]
rs72740674	0.91[EUR][1000 genomes]
rs72740675	0.91[EUR][1000 genomes]
rs72740677	0.91[EUR][1000 genomes]
rs72740679	0.91[EUR][1000 genomes]
rs72740681	0.91[EUR][1000 genomes]
rs72740682	0.91[EUR][1000 genomes]
rs72740683	0.91[EUR][1000 genomes]
rs72740686	0.92[EUR][1000 genomes]
rs72740690	0.91[EUR][1000 genomes]
rs72740691	0.91[EUR][1000 genomes]
rs7701038	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7714993	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7720050	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7723205	0.88[EUR][1000 genomes]
rs7724168	0.91[EUR][1000 genomes];1.00[ASN][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	nsv917332	chr5:26620698-27232713	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv868856	chr5:26789778-27321390	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	3 gene(s)	inside rSNPs	diseases
3	nsv881006	chr5:27010686-27231314	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	esv3450425	chr5:27134073-27323407	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv881286	chr5:27135351-27770554	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv1025795	chr5:27143283-27199590	Enhancers ZNF genes & repeats Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
7	nsv1017638	chr5:27143283-27206186	Weak transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:27158600-27159800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr5:27158800-27160000	Enhancers	HMEC	breast
3	chr5:27159400-27159600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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