Variant report

Variant	rs9493638
Chromosome Location	chr6:133876721-133876722
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11968067	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57743745	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61292016	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61400822	1.00[ASN][1000 genomes]
rs73546895	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73546896	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73546899	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73548803	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73548804	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73548805	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73548813	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7759024	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9402513	1.00[JPT][hapmap]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133873600-133888600	Weak transcription	Ovary	ovary
2	chr6:133876600-133876800	Enhancers	Fetal Stomach	stomach
3	chr6:133876600-133877000	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr6:133876600-133877000	Enhancers	Duodenum Smooth Muscle	Duodenum
5	chr6:133876600-133877000	Enhancers	Fetal Brain Female	brain
6	chr6:133876600-133877200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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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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