Variant report

Variant	rs9350934
Chromosome Location	chr6:82393773-82393774
allele	A/G
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]
rs1156970	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11967364	0.86[AMR][1000 genomes]
rs16893340	0.86[AMR][1000 genomes]
rs72895397	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9359502	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:82391600-82396600	Enhancers	Hela-S3	cervix
2	chr6:82393200-82393800	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr6:82393400-82394200	Enhancers	Muscle Satellite Cultured Cells	--
4	chr6:82393600-82394200	Enhancers	NH-A	brain
5	chr6:82393600-82399600	Weak transcription	Fetal Heart	heart

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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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