Variant report

Variant	rs74059946
Chromosome Location	chr14:69777358-69777359
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1026385	0.95[ASN][1000 genomes]
rs1147471	0.84[ASN][1000 genomes]
rs2185493	0.83[ASN][1000 genomes]
rs2274442	0.93[ASN][1000 genomes]
rs55647841	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55735640	0.91[ASN][1000 genomes]
rs55820856	0.95[ASN][1000 genomes]
rs55926514	0.82[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs56144761	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59831177	1.00[ASN][1000 genomes]
rs877266	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69770200-69778400	Weak transcription	Left Ventricle	heart

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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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