Variant report

Variant	rs588666
Chromosome Location	chr10:117215652-117215653
allele	G/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]
rs12098663	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12098698	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2172668	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs584572	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs604215	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs633750	0.95[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs634209	0.95[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs678632	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs679513	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs681544	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73369798	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:117207200-117220200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr10:117214600-117217000	Weak transcription	Pancreatic Islets	Pancreatic Islet

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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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