Variant report

Variant	rs4890324
Chromosome Location	chr18:43896996-43896997
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10775481	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10853541	0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4890642	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4890643	0.81[ASN][1000 genomes]
rs7232125	0.81[ASN][1000 genomes]
rs9947826	0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9958662	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9960377	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:43894200-43901800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr18:43895600-43899000	Weak transcription	Hela-S3	cervix

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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