Variant report

Variant	rs1281439
Chromosome Location	chr3:59616632-59616633
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs1281447	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1281448	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1281452	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1281458	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1281459	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs937760	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv876836	chr3:59500394-59664687	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv834706	chr3:59538151-59736014	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
3	nsv998711	chr3:59542279-59704503	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	2 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	chr3:59616000-59617800	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr3:59616200-59617000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr3:59616200-59617200	Enhancers	Primary monocytes fromperipheralblood	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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