Variant report

Variant	rs2912520
Chromosome Location	chr8:69979464-69979465
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:69765117..69767304-chr8:69979220..69980795,2	MCF-7	breast:

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10957461	0.95[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs11774986	0.95[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs13252637	0.95[AFR][1000 genomes]
rs1344616	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1344617	0.97[EUR][1000 genomes]
rs1344618	0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs1344619	0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs1365412	0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1365413	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1365414	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1365416	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1365417	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1365418	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1426595	0.95[AFR][1000 genomes]
rs1465514	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1465515	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1541762	0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1559847	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1559848	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1965050	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1965698	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2042732	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2042733	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2042734	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2042735	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2217103	0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs28437123	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2912509	0.93[EUR][1000 genomes]
rs2912510	0.93[EUR][1000 genomes]
rs2912515	1.00[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs2912518	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2912519	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2981041	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2981043	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2981044	0.85[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs2981045	0.93[EUR][1000 genomes]
rs2981047	0.90[AFR][1000 genomes]
rs2981049	0.93[EUR][1000 genomes]
rs2981053	0.95[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs2981056	0.93[EUR][1000 genomes]
rs2981057	0.93[EUR][1000 genomes]
rs2981058	0.93[EUR][1000 genomes]
rs2981059	0.93[EUR][1000 genomes]
rs2981061	0.83[EUR][1000 genomes]
rs2981063	0.93[EUR][1000 genomes]
rs2981065	0.91[EUR][1000 genomes]
rs2981066	0.95[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs34771267	0.95[AFR][1000 genomes]
rs4358809	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs473477	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs608067	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs609760	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs612423	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs623006	0.80[AFR][1000 genomes]
rs625096	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62511793	0.96[ASN][1000 genomes]
rs639293	0.90[CHB][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes]
rs6472436	0.91[EUR][1000 genomes]
rs6472438	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7007693	0.95[AFR][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	nsv1031633	chr8:69766575-70322790	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv890987	chr8:69959105-70004698	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
3	nsv1025578	chr8:69963284-69985807	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:69974000-69980600	Weak transcription	HSMM	muscle
2	chr8:69975600-69979600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr8:69979400-69980000	Enhancers	Osteobl	bone
4	chr8:69979400-69982400	Enhancers	Muscle Satellite Cultured Cells	--

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