Variant report

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

rs_ID	r²[population]
rs10160773	0.80[ASN][1000 genomes]
rs10750631	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10791562	0.82[ASN][1000 genomes]
rs10791563	0.96[EUR][1000 genomes]
rs10895255	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10895256	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11225132	0.92[EUR][1000 genomes]
rs1365331	0.91[EUR][1000 genomes]
rs1426395	0.86[EUR][1000 genomes]
rs1426398	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1549496	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1820453	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2033083	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3752685	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3824930	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61918360	0.85[EUR][1000 genomes]
rs61918361	0.87[EUR][1000 genomes]
rs7106388	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7123006	0.82[ASN][1000 genomes]
rs7931899	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9787758	0.88[EUR][1000 genomes]
rs983112	0.82[AMR][1000 genomes];0.92[EUR][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	esv3362945	chr11:101736547-102114246	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv898333	chr11:101832670-102079986	Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:101968000-101980400	Weak transcription	Right Atrium	heart
2	chr11:101976400-101979800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr11:101978200-101979400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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