Variant report

Variant	rs73105262
Chromosome Location	chr20:16633713-16633714
allele	A/C
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]
rs13040341	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13044376	0.82[AMR][1000 genomes]
rs17682951	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4813234	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs4813236	0.83[EUR][1000 genomes]
rs55712739	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55945497	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56000416	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56324924	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs66517039	0.82[AMR][1000 genomes]
rs73103361	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73103368	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73103369	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73108765	0.82[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:16632800-16634400	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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