Variant report

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

rs_ID	r²[population]
rs10842639	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1167633	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1177523	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1182886	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11836294	0.85[GIH][hapmap]
rs12297557	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12308555	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1495650	0.80[ASN][1000 genomes]
rs16929807	0.85[GIH][hapmap]
rs2643932	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs706514	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs706515	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs706517	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs706540	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs706541	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs829822	0.88[EUR][1000 genomes]
rs829828	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs829833	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs860490	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs865505	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs995796	0.87[EUR][1000 genomes];1.00[ASN][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:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:26076800-26080000	Enhancers	HUVEC	blood vessel
2	chr12:26078000-26081600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr12:26078400-26080200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr12:26078400-26081600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr12:26078400-26081600	Weak transcription	Hela-S3	cervix
6	chr12:26079400-26080000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr12:26079600-26080000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr12:26079600-26080000	Enhancers	NHDF-Ad	bronchial
9	chr12:26079600-26080000	Enhancers	Osteobl	bone
10	chr12:26079600-26082800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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