Variant report

Variant	rs73086944
Chromosome Location	chr1:212024021-212024022
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs17018051	1.00[AMR][1000 genomes]
rs57359943	1.00[AMR][1000 genomes]
rs57845978	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58729775	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59409730	1.00[AMR][1000 genomes]
rs59894091	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61433360	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73084790	1.00[AMR][1000 genomes]
rs73084795	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73086156	1.00[AMR][1000 genomes]
rs73086158	1.00[AMR][1000 genomes]
rs73086164	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73086179	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73086195	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73086199	1.00[AMR][1000 genomes]
rs73086913	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73088107	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73088109	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:212016800-212027000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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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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