Variant report

Variant	rs4280713
Chromosome Location	chr4:120766588-120766589
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10008120	0.97[EUR][1000 genomes]
rs1027691	0.90[EUR][1000 genomes]
rs1027692	0.91[EUR][1000 genomes]
rs10452195	0.95[EUR][1000 genomes]
rs13115558	0.97[EUR][1000 genomes]
rs13141731	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1393967	1.00[EUR][1000 genomes]
rs1503538	0.89[EUR][1000 genomes]
rs17298990	0.97[EUR][1000 genomes]
rs2174170	1.00[EUR][1000 genomes]
rs28690386	0.96[EUR][1000 genomes]
rs4834818	0.96[EUR][1000 genomes]
rs4834819	0.97[EUR][1000 genomes]
rs9991943	0.97[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	nsv916641	chr4:119780023-120777320	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv532739	chr4:120392824-121098103	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120758600-120794000	Weak transcription	Aorta	Aorta

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

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