Variant report

Variant	rs73069331
Chromosome Location	chr2:212637319-212637320
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11897075	0.86[ASN][1000 genomes]
rs56005945	1.00[ASN][1000 genomes]
rs57828323	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58905892	1.00[ASN][1000 genomes]
rs59605575	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62182981	1.00[ASN][1000 genomes]
rs6733874	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73069379	1.00[ASN][1000 genomes]
rs73085038	1.00[ASN][1000 genomes]
rs73085039	1.00[ASN][1000 genomes]
rs73085065	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73085068	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7569623	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7593089	1.00[ASN][1000 genomes]
rs9784129	1.00[ASN][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	esv34128	chr2:212581485-212857122	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	esv3445020	chr2:212636757-212638730	Weak transcription	Chromatin interactive region	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	chr2:212633200-212638000	Weak transcription	Aorta	Aorta

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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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