Variant report

Variant	rs62179348
Chromosome Location	chr1:71190667-71190668
allele	A/C/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]
rs1432290	0.82[ASN][1000 genomes]
rs1653793	0.82[ASN][1000 genomes]
rs1653798	0.84[ASN][1000 genomes]
rs1669462	0.80[ASN][1000 genomes]
rs1669464	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1669466	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1669467	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1901430	0.80[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4953889	0.83[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs4954071	0.84[ASN][1000 genomes]
rs6716417	0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7425932	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7561974	0.83[ASN][1000 genomes]
rs7574382	0.86[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:71184000-71193000	Weak transcription	Aorta	Aorta

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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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