Variant report

Variant	rs73987541
Chromosome Location	chr2:209455459-209455460
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]
rs55974317	0.90[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs56199915	0.90[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs56325500	0.93[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs72985935	0.93[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72985936	0.82[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs72985938	0.90[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs72985950	0.90[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs73987539	0.93[AFR][1000 genomes];0.87[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209438800-209459400	Weak transcription	K562	blood
2	chr2:209449400-209458800	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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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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