Variant report

Variant	rs72788558
Chromosome Location	chr2:21194868-21194869
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs10164442	0.87[ASN][1000 genomes]
rs10172650	0.87[ASN][1000 genomes]
rs11124924	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72780134	0.84[ASN][1000 genomes]
rs72788559	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:21189600-21195000	Weak transcription	Aorta	Aorta
2	chr2:21194000-21195000	Weak transcription	Stomach Smooth Muscle	stomach
3	chr2:21194400-21195600	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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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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