Variant report

Variant	rs34533513
Chromosome Location	chr3:155744312-155744313
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11706897	0.84[ASN][1000 genomes]
rs11714137	0.98[EUR][1000 genomes]
rs11719280	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4680230	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6806030	0.83[EUR][1000 genomes]
rs6806441	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs71310459	0.94[EUR][1000 genomes]
rs7643130	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs883670	0.80[EUR][1000 genomes]
rs9875491	0.84[ASN][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:155738200-155748600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr3:155743400-155748200	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr3:155743400-155748600	Weak transcription	HUES6 Cell Line	embryonic stem cell

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Input of quick search could be:

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

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