Variant report

Variant	rs34456987
Chromosome Location	chr8:42523329-42523330
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	chr8:42519069..42520896-chr8:42522554..42525059,2	MCF-7	breast:
2	chr8:42519696..42522566-chr8:42522685..42524455,2	K562	blood:

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10958725	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10958727	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13254578	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13273442	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13277254	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13277524	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13280604	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1451239	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1451240	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs16891561	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1901281	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1955185	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1955186	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1979140	0.98[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35599391	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs36057318	0.80[ASN][1000 genomes]
rs4236926	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4295650	0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4736835	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4736838	0.80[EUR][1000 genomes]
rs4950	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4951	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs55828312	0.83[EUR][1000 genomes]
rs57645595	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs58379124	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6474411	0.82[EUR][1000 genomes]
rs6474412	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6474413	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6474414	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6474415	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6985052	0.95[AFR][1000 genomes];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6990603	0.83[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6997909	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7004381	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7459838	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7837296	0.80[ASN][1000 genomes]
rs7842601	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9643853	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9643891	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9692914	0.86[AFR][1000 genomes]
rs9693825	0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9693858	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9792257	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9792277	0.84[AMR][1000 genomes];0.88[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	nsv530880	chr8:41895241-42755506	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv1034724	chr8:42386707-42772203	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:42522200-42533400	Weak transcription	Dnd41	blood

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