Variant report

Variant	rs73918003
Chromosome Location	chr2:21148126-21148127
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs55900088	0.83[AMR][1000 genomes]
rs56164002	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61079625	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6747634	0.85[AMR][1000 genomes]
rs73918005	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73918008	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73918011	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73921326	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73921332	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73921339	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73921340	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7594128	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:21133400-21149400	Weak transcription	H1 Derived Mesenchymal Stem 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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