Variant report

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

rs_ID	r²[population]
rs1978873	1.00[ASN][1000 genomes]
rs55988377	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56232132	1.00[ASN][1000 genomes]
rs62182978	1.00[ASN][1000 genomes]
rs6715164	1.00[ASN][1000 genomes]
rs6752616	1.00[ASN][1000 genomes]
rs72933724	1.00[ASN][1000 genomes]
rs72933726	1.00[ASN][1000 genomes]
rs72933730	1.00[ASN][1000 genomes]
rs72933731	1.00[ASN][1000 genomes]
rs72933735	1.00[ASN][1000 genomes]
rs72933744	1.00[ASN][1000 genomes]
rs72945031	1.00[ASN][1000 genomes]
rs72945032	1.00[ASN][1000 genomes]
rs72945039	1.00[ASN][1000 genomes]
rs72945086	1.00[ASN][1000 genomes]
rs72945096	1.00[ASN][1000 genomes]
rs72945099	1.00[ASN][1000 genomes]
rs72946524	1.00[ASN][1000 genomes]
rs72946542	1.00[ASN][1000 genomes]
rs72946560	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34128	chr2:212581485-212857122	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212610200-212626600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr2:212617000-212620800	Weak transcription	Fetal Lung	lung

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