Variant report

Variant	rs6563150
Chromosome Location	chr13:80501104-80501105
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 82 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:79)

rs_ID	r²[population]
rs11838566	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11840618	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11840648	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11840740	0.96[ASN][1000 genomes]
rs11841357	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11843138	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12323034	0.90[ASN][1000 genomes]
rs12323035	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12583025	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12583645	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12585712	0.85[AMR][1000 genomes]
rs12853769	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12861375	0.97[ASN][1000 genomes]
rs12867413	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12868561	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12876835	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13378771	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1811362	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2007276	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2118798	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2304638	0.94[ASN][1000 genomes]
rs2329003	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2329148	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs34622893	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs34710670	0.90[ASN][1000 genomes]
rs36063327	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3850061	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3850062	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3850064	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3861143	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3861144	0.90[ASN][1000 genomes]
rs3898550	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3898551	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3916021	0.84[ASN][1000 genomes]
rs4052505	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4514565	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4533153	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4884141	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4884142	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4885683	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs55978445	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs57067871	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6563146	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs66994466	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7318554	0.85[ASN][1000 genomes]
rs7329042	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7329614	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7330635	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7332417	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7333212	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7336725	0.94[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7982819	0.98[ASN][1000 genomes]
rs7994328	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7995887	0.86[ASN][1000 genomes]
rs7997147	0.97[ASN][1000 genomes]
rs9318660	0.82[ASN][1000 genomes]
rs9318662	0.91[ASN][1000 genomes]
rs9318663	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9545261	0.88[ASN][1000 genomes]
rs9545268	0.98[ASN][1000 genomes]
rs9593417	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9593418	0.82[ASN][1000 genomes]
rs9593419	0.83[EUR][1000 genomes]
rs9593420	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9593421	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9601280	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9601281	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9601283	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9601285	0.82[EUR][1000 genomes]
rs9601286	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9601288	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9601289	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9601290	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9601291	0.86[ASN][1000 genomes]
rs9601293	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9601294	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs9805460	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs996823	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs996824	0.89[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:3 , 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
3	chr13:80500800-80501800	Enhancers	HUVEC	blood vessel

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