Variant report

Variant	rs59961456
Chromosome Location	chr11:32392844-32392845
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs16923250	0.85[AFR][1000 genomes]
rs16923260	0.84[AFR][1000 genomes]
rs2234593	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs28460016	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5030228	0.85[AFR][1000 genomes]
rs5030278	0.86[ASN][1000 genomes]
rs5030302	0.86[ASN][1000 genomes]
rs5030311	0.84[AMR][1000 genomes]
rs5030315	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs5030316	0.90[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs5030335	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7105471	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7120483	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72896061	0.80[EUR][1000 genomes]
rs72896066	0.80[EUR][1000 genomes]
rs72896067	0.80[EUR][1000 genomes]
rs73473736	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[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	esv3375305	chr11:32388061-32395369	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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