Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs12213780	0.80[ASN][1000 genomes]
rs12664883	0.99[ASN][1000 genomes]
rs1321723	1.00[ASN][1000 genomes]
rs1321734	0.81[ASN][1000 genomes]
rs1321735	0.80[ASN][1000 genomes]
rs1321736	0.80[ASN][1000 genomes]
rs1407159	0.81[ASN][1000 genomes]
rs1407161	0.80[ASN][1000 genomes]
rs1926019	0.81[ASN][1000 genomes]
rs2146272	0.80[ASN][1000 genomes]
rs4141965	0.80[ASN][1000 genomes]
rs486470	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs504392	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs505007	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs510422	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs536094	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs541665	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs562034	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs563365	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs572893	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs575779	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6925525	0.80[ASN][1000 genomes]
rs7745528	0.81[ASN][1000 genomes]
rs7768040	0.80[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	nsv1017418	chr6:85344786-86259540	Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Enhancers Bivalent/Poised TSS Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv538347	chr6:85344786-86259540	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:85834000-85838400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr6:85837600-85840400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr6:85837600-85845600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr6:85837800-85839600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr6:85838000-85838400	Weak transcription	NHDF-Ad	bronchial
6	chr6:85838000-85838800	Weak transcription	Osteobl	bone
7	chr6:85838000-85840800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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