Variant report

Variant	rs10055632
Chromosome Location	chr5:91739565-91739566
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]
rs10041056	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10041199	1.00[ASN][1000 genomes]
rs10052520	1.00[ASN][1000 genomes]
rs10055515	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10057380	0.92[AFR][1000 genomes]
rs10063190	0.92[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs10065964	0.92[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs10073874	0.95[EUR][1000 genomes]
rs13354246	0.92[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs72777068	0.95[EUR][1000 genomes]
rs72777069	0.95[EUR][1000 genomes]
rs72777081	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:91738600-91739600	Weak transcription	Fetal Brain Female	brain

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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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