Variant report

Variant	rs73672192
Chromosome Location	chr8:34149701-34149702
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs16881980	0.81[EUR][1000 genomes]
rs16882075	0.85[AMR][1000 genomes]
rs16882130	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs28703850	0.81[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs55935531	0.81[EUR][1000 genomes]
rs55958437	0.81[EUR][1000 genomes]
rs59851071	0.81[EUR][1000 genomes]
rs61505297	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73672188	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73672189	0.83[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs73672194	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73674307	0.81[EUR][1000 genomes]
rs73674308	0.81[EUR][1000 genomes]
rs7839209	0.86[AFR][1000 genomes];0.81[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:34149200-34152600	Weak transcription	Fetal Brain Male	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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