Variant report

Variant	rs1589949
Chromosome Location	chr2:76519823-76519824
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11684308	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12713866	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13006506	0.87[AFR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13422380	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1405338	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1526620	0.93[AFR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1526627	0.81[AFR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1526654	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs67297254	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs67356654	0.87[AFR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs67363452	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:76508800-76520200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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