Variant report

Variant	rs36054909
Chromosome Location	chr2:209441694-209441695
allele	A/G
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]
rs10205358	0.94[EUR][1000 genomes]
rs13016164	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13032946	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13035863	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs16841273	1.00[AMR][1000 genomes]
rs34029972	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34661013	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs34757991	1.00[AMR][1000 genomes]
rs5028247	1.00[EUR][1000 genomes]
rs6704611	1.00[EUR][1000 genomes]
rs6749067	1.00[EUR][1000 genomes]
rs71418693	1.00[AMR][1000 genomes]
rs71418695	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71418697	1.00[EUR][1000 genomes]
rs7557972	1.00[EUR][1000 genomes]
rs9808325	0.94[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209438800-209459400	Weak transcription	K562	blood

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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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