Variant report

Variant	rs72907573
Chromosome Location	chr11:32394605-32394606
allele	C/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]
rs5030267	0.81[AMR][1000 genomes]
rs5030276	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs5030308	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs5030309	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs5030322	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs5030331	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72907570	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72907575	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72907578	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72907581	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72907582	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72907585	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72907590	0.93[EUR][1000 genomes]
rs72907594	0.93[EUR][1000 genomes]
rs72907595	0.93[EUR][1000 genomes]
rs72907600	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72907602	1.00[AMR][1000 genomes];0.93[EUR][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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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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