Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10187570	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10198544	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10205429	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1074149	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12465694	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13414651	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1601359	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17197940	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1843269	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1905742	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2062363	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2062364	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2342552	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4374368	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs56317281	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62169063	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62169068	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62169088	0.89[ASN][1000 genomes]
rs720066	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs749691	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525350	chr2:151711700-152044794	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv523849	chr2:151718133-152143524	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	esv3693426	chr2:151725792-152295862	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
4	nsv1002140	chr2:151833257-152054910	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:151940000-151942800	Enhancers	Fetal Stomach	stomach
2	chr2:151941000-151943200	Enhancers	Fetal Lung	lung
3	chr2:151941600-151943600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr2:151941600-151943800	Weak transcription	Primary T cells from cord blood	blood
5	chr2:151942400-151943600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr2:151942400-151958800	Weak transcription	Fetal Brain Female	brain

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