Variant report

Variant	rs9318663
Chromosome Location	chr13:80503110-80503111
allele	A/C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 80 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs11838566	0.91[EUR][1000 genomes]
rs11840618	0.84[EUR][1000 genomes]
rs11840648	0.84[EUR][1000 genomes]
rs11840740	0.94[ASN][1000 genomes]
rs11841357	0.91[EUR][1000 genomes]
rs11843138	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12323034	0.88[ASN][1000 genomes]
rs12323035	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12583025	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12583645	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12585712	0.82[EUR][1000 genomes]
rs12853769	0.84[EUR][1000 genomes]
rs12861375	0.94[ASN][1000 genomes]
rs12867413	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12868561	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12876835	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13378771	0.94[EUR][1000 genomes]
rs1811362	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2007276	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2118798	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2304638	0.91[ASN][1000 genomes]
rs2329003	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2329148	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs34622893	0.85[EUR][1000 genomes]
rs34710670	0.88[ASN][1000 genomes]
rs36063327	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3850061	0.91[EUR][1000 genomes]
rs3850062	0.91[EUR][1000 genomes]
rs3850064	0.91[EUR][1000 genomes]
rs3861143	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3861144	0.89[ASN][1000 genomes]
rs3898550	0.96[EUR][1000 genomes]
rs3898551	0.96[EUR][1000 genomes]
rs3916021	0.82[ASN][1000 genomes]
rs4052505	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4514565	0.93[EUR][1000 genomes]
rs4533153	0.95[EUR][1000 genomes]
rs4884141	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4884142	0.96[EUR][1000 genomes]
rs4885683	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55978445	0.91[EUR][1000 genomes]
rs57067871	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6563146	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6563150	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs66994466	0.84[EUR][1000 genomes]
rs7318554	0.85[ASN][1000 genomes]
rs7329042	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7329614	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7330635	0.96[EUR][1000 genomes]
rs7332417	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7333212	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7336725	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7982819	0.95[ASN][1000 genomes]
rs7994328	0.84[EUR][1000 genomes]
rs7995887	0.85[ASN][1000 genomes]
rs7997147	0.94[ASN][1000 genomes]
rs9318662	0.91[ASN][1000 genomes]
rs9545261	0.87[ASN][1000 genomes]
rs9545268	0.93[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs9593417	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9593419	0.84[EUR][1000 genomes]
rs9593420	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9593421	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9601280	0.91[EUR][1000 genomes]
rs9601281	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9601283	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9601285	0.85[EUR][1000 genomes]
rs9601286	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9601288	0.96[EUR][1000 genomes]
rs9601289	0.93[EUR][1000 genomes]
rs9601290	0.96[EUR][1000 genomes]
rs9601291	0.85[ASN][1000 genomes]
rs9601293	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9601294	0.95[ASN][1000 genomes]
rs9805460	0.89[EUR][1000 genomes]
rs996823	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs996824	0.84[AMR][1000 genomes];0.92[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	nsv438256	chr13:80479404-80503110	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv832658	chr13:80486980-80680221	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv562417	chr13:80489814-80618915	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:80493200-80504600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr13:80498800-80510400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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