Variant report

Variant	rs9969592
Chromosome Location	chr8:122025559-122025560
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	chr8:122010810..122013108-chr8:122024676..122026870,2	MCF-7	breast:

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs12676933	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12678662	0.88[ASN][1000 genomes]
rs12680902	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12681516	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1347231	0.88[ASN][1000 genomes]
rs1368603	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1433397	1.00[ASN][1000 genomes]
rs1594742	0.88[ASN][1000 genomes]
rs1594743	0.87[ASN][1000 genomes]
rs1631099	1.00[ASN][1000 genomes]
rs16894516	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16894530	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16894534	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1714642	0.97[ASN][1000 genomes]
rs1714653	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1812421	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1865180	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2043373	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2043377	0.90[ASN][1000 genomes]
rs2068952	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2117063	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2117064	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2163922	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4871152	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4871154	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4871155	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4871156	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4871157	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4871158	0.88[ASN][1000 genomes]
rs4871159	0.87[ASN][1000 genomes]
rs6469984	1.00[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6469985	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6469986	1.00[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6469987	1.00[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6982541	0.88[ASN][1000 genomes]
rs7003498	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7007419	1.00[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs7012535	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73315279	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73317195	0.90[ASN][1000 genomes]
rs73318915	0.90[ASN][1000 genomes]
rs73318932	0.88[ASN][1000 genomes]
rs961427	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs961428	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9774583	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv465790	chr8:121853405-122185415	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv612114	chr8:121853405-122185415	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv891424	chr8:121873345-122393258	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv891425	chr8:121875083-122025559	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	esv1844734	chr8:121928250-122283585	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr8:122024400-122026200	Enhancers	HepG2	liver

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