Variant report

Variant	rs11746665
Chromosome Location	chr5:108447368-108447369
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10040959	0.81[EUR][1000 genomes]
rs10056058	0.81[EUR][1000 genomes]
rs10063845	0.81[EUR][1000 genomes]
rs10070411	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10073414	0.91[ASN][1000 genomes]
rs10085093	0.89[EUR][1000 genomes]
rs10477944	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10477946	0.86[EUR][1000 genomes]
rs10477947	0.87[EUR][1000 genomes]
rs10477948	0.87[EUR][1000 genomes]
rs10477949	0.87[EUR][1000 genomes]
rs10477952	0.87[EUR][1000 genomes]
rs17450345	0.86[ASN][1000 genomes]
rs17450387	0.81[EUR][1000 genomes]
rs17450455	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17473391	0.84[EUR][1000 genomes]
rs2195944	0.90[EUR][1000 genomes]
rs2217649	0.89[EUR][1000 genomes]
rs2416198	0.85[EUR][1000 genomes]
rs2416200	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28699553	0.90[EUR][1000 genomes]
rs3816024	0.95[ASN][1000 genomes]
rs4957567	0.89[EUR][1000 genomes]
rs4957799	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs55930293	0.87[EUR][1000 genomes]
rs55953478	0.90[EUR][1000 genomes]
rs57196331	0.89[EUR][1000 genomes]
rs57960033	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs59337218	0.85[EUR][1000 genomes]
rs6872780	0.89[EUR][1000 genomes]
rs73779027	0.90[EUR][1000 genomes]
rs73779053	0.86[EUR][1000 genomes]
rs73779135	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9326759	0.89[EUR][1000 genomes]
rs9326760	0.90[EUR][1000 genomes]
rs9326762	0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830443	chr5:108326491-108496723	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
2	nsv882692	chr5:108391660-108474166	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv882693	chr5:108391660-108502493	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv882694	chr5:108391660-108524416	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	nsv4953	chr5:108443905-108488747	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1027163	chr5:108445447-108839913	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:108441600-108447400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr5:108441600-108455600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr5:108441800-108455600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr5:108442000-108497400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr5:108442400-108449000	Weak transcription	Pancreas	Pancrea
6	chr5:108442800-108455600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr5:108444200-108455600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr5:108445800-108448200	Weak transcription	Primary B cells from cord blood	blood
9	chr5:108446800-108447800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr5:108447000-108447800	Enhancers	HUVEC	blood vessel

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links