Variant report

Variant	rs2066351
Chromosome Location	chr6:119790978-119790979
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:119789332..119793434-chr6:119796076..119800106,5	K562	blood:
2	chr6:119789925..119791894-chr6:119924066..119925915,2	MCF-7	breast:
3	chr6:119789748..119793434-chr6:119796076..119799168,3	K562	blood:

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs11153826	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12528127	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1342313	0.81[AMR][1000 genomes]
rs1909506	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1995224	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2153825	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2357505	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4945638	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4946416	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4946421	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4946428	1.00[CEU][hapmap];0.86[CHB][hapmap];0.81[JPT][hapmap];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4946430	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs58391013	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6900388	0.81[AMR][1000 genomes]
rs6925366	0.84[AMR][1000 genomes]
rs6935847	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6936821	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs72952941	0.81[AMR][1000 genomes]
rs7761301	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7774019	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs885028	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9374797	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9374798	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9374799	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9374800	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9374801	1.00[CEU][hapmap];0.86[CHB][hapmap];0.81[JPT][hapmap];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9374802	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9374803	1.00[CEU][hapmap];0.94[CHB][hapmap];0.84[JPT][hapmap];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9385074	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9385075	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9387650	0.81[AMR][1000 genomes]
rs9387654	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9401149	0.94[AMR][1000 genomes];0.88[EUR][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	esv3447598	chr6:119558591-120119384	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	esv3389526	chr6:119558598-120190087	ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv1027904	chr6:119709488-120001986	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv533518	chr6:119712186-119998618	ZNF genes & repeats Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	esv3442553	chr6:119742069-120076777	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:119789600-119792400	Weak transcription	K562	blood
2	chr6:119789600-119793800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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