Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10771247	0.82[AMR][1000 genomes]
rs1167618	0.80[AMR][1000 genomes]
rs1177524	0.83[AMR][1000 genomes]
rs1183807	0.83[AMR][1000 genomes]
rs1488826	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1488827	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1797965	0.83[AMR][1000 genomes]
rs2634170	0.83[AMR][1000 genomes]
rs2643928	0.83[AMR][1000 genomes]
rs4246236	0.83[AMR][1000 genomes]
rs4246237	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs4473022	0.88[CHB][hapmap];0.83[AMR][1000 genomes]
rs706539	0.83[AMR][1000 genomes]
rs7134761	0.88[JPT][hapmap]
rs7298011	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7954454	0.94[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs829823	0.83[AMR][1000 genomes]
rs829825	0.83[AMR][1000 genomes]
rs829826	0.83[AMR][1000 genomes]
rs829827	0.83[AMR][1000 genomes]
rs844202	0.83[AMR][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	esv2758300	chr12:25992331-26161116	Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	38 gene(s)	inside rSNPs	diseases
2	esv2759886	chr12:25992331-26161116	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	38 gene(s)	inside rSNPs	diseases
3	nsv1035319	chr12:26020667-26097148	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:26039200-26044400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:26043200-26045400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr12:26044200-26044400	Weak transcription	NHEK	skin

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