Variant report

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

rs_ID	r²[population]
rs1156409	0.88[EUR][1000 genomes]
rs12196125	0.89[ASN][1000 genomes]
rs1486605	0.88[EUR][1000 genomes]
rs16881433	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs16881449	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs16881450	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16881458	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16881463	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2087093	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2881952	0.88[EUR][1000 genomes]
rs3920742	0.88[EUR][1000 genomes]
rs4707928	0.92[EUR][1000 genomes]
rs56699974	0.81[EUR][1000 genomes]
rs62404040	0.89[ASN][1000 genomes]
rs6453557	0.88[EUR][1000 genomes]
rs73747164	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73747165	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73747166	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9293845	0.88[EUR][1000 genomes]
rs9442674	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9446403	0.88[EUR][1000 genomes];0.89[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	nsv830684	chr6:72094842-72282684	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	488 gene(s)	inside rSNPs	diseases
2	esv2763575	chr6:72227746-72240130	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:72236000-72239400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:72238000-72239600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr6:72238000-72241800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr6:72238400-72239600	Weak transcription	Placenta Amnion	Placenta Amnion

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