Variant report

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs1455265	1.00[EUR][1000 genomes]
rs17027850	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17027873	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17027894	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17027897	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17027899	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17027901	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17027902	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17027903	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17027906	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17027922	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17028098	1.00[EUR][1000 genomes]
rs56778186	0.88[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs57272995	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57360299	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57518057	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57702773	1.00[EUR][1000 genomes]
rs57840658	1.00[EUR][1000 genomes]
rs58051386	1.00[EUR][1000 genomes]
rs58695205	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58718173	1.00[EUR][1000 genomes]
rs59718895	1.00[EUR][1000 genomes]
rs59969247	1.00[EUR][1000 genomes]
rs59973565	1.00[EUR][1000 genomes]
rs60215951	1.00[EUR][1000 genomes]
rs60413056	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60600949	1.00[EUR][1000 genomes]
rs61165969	1.00[EUR][1000 genomes]
rs6747989	1.00[EUR][1000 genomes]
rs7603484	1.00[EUR][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	esv1800788	chr2:63473443-63900292	ZNF genes & repeats Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:63768600-63777400	Weak transcription	Primary hematopoietic stem cells	blood
2	chr2:63772800-63788800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr2:63773200-63783200	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr2:63774800-63780000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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