Variant report

Variant	rs9862740
Chromosome Location	chr3:139882072-139882073
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	chr3:139878853..139881131-chr3:139881618..139884130,2	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs12634879	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1316385	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1317898	0.90[EUR][1000 genomes]
rs1320256	0.88[EUR][1000 genomes]
rs1320259	0.90[EUR][1000 genomes]
rs1320260	0.90[EUR][1000 genomes]
rs2350275	0.90[EUR][1000 genomes]
rs2350276	0.83[EUR][1000 genomes]
rs2350281	0.84[EUR][1000 genomes]
rs2350508	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2350509	0.88[EUR][1000 genomes]
rs2882369	0.90[EUR][1000 genomes]
rs2882370	0.84[EUR][1000 genomes]
rs4317058	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4596106	0.85[EUR][1000 genomes]
rs4683480	0.83[EUR][1000 genomes]
rs4683481	0.91[EUR][1000 genomes]
rs4683808	0.90[EUR][1000 genomes]
rs6439899	0.91[EUR][1000 genomes]
rs6791658	0.90[EUR][1000 genomes]
rs6796645	0.83[EUR][1000 genomes]
rs7355921	0.91[EUR][1000 genomes]
rs7645343	0.90[EUR][1000 genomes]
rs9283594	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9289599	0.83[EUR][1000 genomes]
rs939189	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs939190	0.91[EUR][1000 genomes]
rs9817495	0.91[EUR][1000 genomes]
rs9818360	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9818488	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9822943	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9823483	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9855981	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9862768	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9868890	0.90[EUR][1000 genomes]
rs9871857	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9873081	0.88[EUR][1000 genomes]
rs9873941	0.98[EUR][1000 genomes]
rs9878323	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9990262	0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv998423	chr3:139526446-139947336	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv829739	chr3:139797496-140002685	Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:139867400-139890000	Weak transcription	HSMMtube	muscle
2	chr3:139877000-139901200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr3:139879800-139883600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr3:139879800-139883800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr3:139880200-139886400	Weak transcription	NHDF-Ad	bronchial
6	chr3:139881600-139884200	Weak transcription	Ovary	ovary

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