Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10485244	0.80[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs17766479	0.87[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2096058	0.91[ASN][1000 genomes]
rs3793036	0.87[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs3805961	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3805962	0.92[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs3805966	0.92[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs3805968	0.92[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs3805971	0.92[AMR][1000 genomes]
rs3805973	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3805977	0.95[ASN][1000 genomes]
rs56922945	0.82[ASN][1000 genomes]
rs59707679	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs60134810	0.93[ASN][1000 genomes]
rs6938320	0.80[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs7761968	0.80[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs9446169	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9446170	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9446172	0.97[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9446178	0.89[ASN][1000 genomes]
rs9454910	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9454914	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][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	nsv886140	chr6:70354682-70728202	Strong transcription Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv886141	chr6:70590638-70694162	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:70601600-70604200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr6:70602000-70603800	Weak transcription	Primary B cells from peripheral blood	blood
3	chr6:70602000-70604000	Weak transcription	GM12878-XiMat	blood
4	chr6:70602000-70604400	Weak transcription	Primary B cells from cord blood	blood
5	chr6:70602000-70604800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr6:70602400-70604600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr6:70602600-70603200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr6:70602600-70603400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr6:70602600-70604800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr6:70602800-70603600	Weak transcription	Adipose Nuclei	Adipose
11	chr6:70602800-70605200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr6:70602800-70605200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr6:70603000-70605000	Enhancers	Fetal Heart	heart
14	chr6:70603000-70605200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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