Variant report

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

rs_ID	r²[population]
rs10085172	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12527395	0.89[ASN][1000 genomes]
rs12528003	0.83[EUR][1000 genomes]
rs17083610	0.85[JPT][hapmap]
rs1925220	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs2038836	0.83[EUR][1000 genomes]
rs2038837	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2147709	0.87[ASN][1000 genomes]
rs4945685	0.82[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs4946568	0.83[EUR][1000 genomes]
rs5012746	0.83[EUR][1000 genomes]
rs56308178	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs67612546	0.84[ASN][1000 genomes]
rs68192738	0.84[ASN][1000 genomes]
rs6903232	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7740324	0.85[JPT][hapmap]
rs7740467	0.84[JPT][hapmap]
rs7775464	0.88[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs7775586	0.89[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs9490222	1.00[CHB][hapmap];0.83[JPT][hapmap]
rs9490225	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs9490226	1.00[CHB][hapmap];0.83[JPT][hapmap]
rs9490238	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9490239	0.97[AMR][1000 genomes];1.00[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	nsv530527	chr6:121298528-121789855	ZNF genes & repeats Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv830789	chr6:121581450-121732320	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:121727400-121731600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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