Variant report

Variant	rs2912509
Chromosome Location	chr8:69962007-69962008
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:69958015..69960106-chr8:69960597..69962712,2	MCF-7	breast:

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10957460	1.00[ASN][1000 genomes]
rs10957461	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11774986	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13252637	0.99[ASN][1000 genomes]
rs13272381	0.87[ASN][1000 genomes]
rs1344616	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1344617	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1344618	0.95[CHB][hapmap]
rs1344619	0.95[CHB][hapmap]
rs1365413	0.96[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs1365414	0.96[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs1365416	0.93[EUR][1000 genomes]
rs1365417	0.96[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs1365418	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1426595	1.00[ASN][1000 genomes]
rs1465514	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1465515	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1559847	0.96[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs1559848	0.96[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs1965050	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1965698	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2042732	0.96[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs2042733	0.96[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs2042734	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2042735	0.96[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs2162353	1.00[ASN][1000 genomes]
rs28437123	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2912510	0.80[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2912515	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2912518	0.96[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs2912519	0.96[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs2912520	0.93[EUR][1000 genomes]
rs2981041	0.96[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs2981043	0.96[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs2981045	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2981047	1.00[ASN][1000 genomes]
rs2981049	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2981053	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2981056	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2981057	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2981058	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2981059	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2981061	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2981062	1.00[ASN][1000 genomes]
rs2981063	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2981065	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2981066	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34771267	1.00[ASN][1000 genomes]
rs4358809	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs473477	1.00[CEU][hapmap];0.95[CHB][hapmap];0.89[YRI][hapmap];0.96[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs608067	1.00[CEU][hapmap];0.95[CHB][hapmap];0.89[YRI][hapmap];0.96[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs609760	1.00[CEU][hapmap];0.95[CHB][hapmap];0.89[YRI][hapmap];0.96[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs612423	0.95[CHB][hapmap]
rs625096	0.96[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs639293	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6472436	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6472438	0.96[AFR][1000 genomes];0.99[EUR][1000 genomes]
rs7007693	1.00[ASN][1000 genomes]
rs7835428	1.00[ASN][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	esv3438905	chr8:69961863-69962057	Enhancers Weak transcription	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	chr8:69960400-69973600	Weak transcription	HSMM	muscle
2	chr8:69961000-69962200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr8:69961000-69962400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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