Variant report

Variant	rs11626516
Chromosome Location	chr14:63260004-63260005
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10162511	0.88[ASN][1000 genomes]
rs11844092	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11848421	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11851665	0.97[ASN][1000 genomes]
rs11851948	0.90[ASN][1000 genomes]
rs1809676	0.81[ASN][1000 genomes]
rs1844511	0.81[ASN][1000 genomes]
rs1873274	0.82[ASN][1000 genomes]
rs1971271	0.98[ASN][1000 genomes]
rs1977631	0.88[ASN][1000 genomes]
rs6573461	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7152953	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7154517	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7161467	0.82[ASN][1000 genomes]
rs761855	0.96[ASN][1000 genomes]
rs8005419	0.81[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:63255600-63274400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	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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