Variant report

Variant	rs336246
Chromosome Location	chr13:110481449-110481450
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs170860	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1999710	0.84[EUR][1000 genomes]
rs336229	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs336230	0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs336238	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs336242	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs336247	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4238270	0.82[EUR][1000 genomes]
rs4771653	0.86[EUR][1000 genomes]
rs752946	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9521523	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:110473800-110489200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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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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