Variant report

Variant	rs73867446
Chromosome Location	chr3:146347151-146347152
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs12107687	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16858483	1.00[AMR][1000 genomes]
rs16858513	1.00[AMR][1000 genomes]
rs16858523	1.00[AMR][1000 genomes]
rs16858568	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16858582	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28429720	1.00[AMR][1000 genomes]
rs41414448	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55796696	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73865809	1.00[AMR][1000 genomes]
rs73865812	1.00[AMR][1000 genomes]
rs73865817	1.00[AMR][1000 genomes]
rs73867434	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73867436	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73867437	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:146344600-146351000	Weak transcription	Colon Smooth Muscle	Colon
2	chr3:146346000-146350800	Weak transcription	HepG2	liver

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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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