Variant report

Variant	rs58649746
Chromosome Location	chr2:73351806-73351807
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1046183	0.86[ASN][1000 genomes]
rs13404068	0.83[ASN][1000 genomes]
rs2421099	0.85[ASN][1000 genomes]
rs56931614	0.93[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs56992198	0.94[ASN][1000 genomes]
rs57875548	0.88[ASN][1000 genomes]
rs58469852	0.83[ASN][1000 genomes]
rs58617186	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs58659495	0.87[ASN][1000 genomes]
rs59802755	0.90[ASN][1000 genomes]
rs60341789	0.98[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs61061024	0.88[ASN][1000 genomes]
rs6716846	0.85[ASN][1000 genomes]
rs67421457	0.86[AFR][1000 genomes];0.91[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	nsv1006801	chr2:73305056-73431711	Weak transcription Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr2:73345600-73356200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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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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