Variant report

Variant	rs4269255
Chromosome Location	chr5:68298522-68298523
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs12656917	0.81[ASN][1000 genomes]
rs3922936	0.81[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs3922937	0.83[ASN][1000 genomes]
rs4373240	0.81[ASN][1000 genomes]
rs4432834	0.86[ASN][1000 genomes]
rs4594812	0.81[ASN][1000 genomes]
rs4976004	0.81[ASN][1000 genomes]
rs4976007	0.81[ASN][1000 genomes]
rs4976056	0.81[ASN][1000 genomes]
rs4976068	0.81[ASN][1000 genomes]
rs5022687	0.81[ASN][1000 genomes]
rs5022688	0.81[ASN][1000 genomes]
rs6874327	0.81[ASN][1000 genomes]
rs6887916	0.81[ASN][1000 genomes]
rs7732834	0.81[ASN][1000 genomes]
rs7733298	0.83[ASN][1000 genomes]
rs7733454	0.83[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	esv2763462	chr5:68295338-68307023	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:68298000-68301600	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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