Variant report

Variant	rs59311105
Chromosome Location	chr2:100136759-100136760
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs17022741	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17022788	0.83[EUR][1000 genomes]
rs2167339	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3087387	1.00[AMR][1000 genomes]
rs56684522	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57093686	1.00[AMR][1000 genomes]
rs57599963	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57668619	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs57969550	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58226642	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58780429	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59753430	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59859749	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60633946	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6707685	1.00[AMR][1000 genomes]
rs6723062	1.00[AMR][1000 genomes]
rs6745673	0.83[EUR][1000 genomes]
rs6761053	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6761507	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73964150	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73964151	0.83[AMR][1000 genomes]
rs73964152	1.00[AMR][1000 genomes]
rs73964155	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73964157	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73964158	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73964166	0.83[EUR][1000 genomes]
rs7568990	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7570405	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7571186	1.00[AMR][1000 genomes]
rs7595242	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[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	nsv431424	chr2:99652682-100494682	Flanking Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv962113	chr2:100022168-100317461	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 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	chr2:100136200-100140600	Weak transcription	Fetal Heart	heart
2	chr2:100136600-100136800	Weak transcription	Primary neutrophils fromperipheralblood	blood

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