Variant report

Variant	rs7667055
Chromosome Location	chr4:106804450-106804451
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11933393	0.97[AFR][1000 genomes]
rs2544400	0.97[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs2544406	0.97[AFR][1000 genomes]
rs2544408	0.96[AFR][1000 genomes]
rs2544410	0.96[AFR][1000 genomes]
rs2544425	0.97[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs2553434	0.98[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs2553437	0.88[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs2553472	0.98[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs4456959	0.99[ASN][1000 genomes]
rs4579125	0.99[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	nsv1014993	chr4:106796019-106980727	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 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	chr4:106792200-106815800	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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