Table 1 Single nucleotide polymorphisms associated with high blood pressure located in regions containing copy number variation (Build hg19, based on the Database for Genomic Variants and UCSC Genome Browser, search performed on 28 May 2014)
From: Measurement of absolute copy number variation reveals association with essential hypertension
SNP ID | CNV ID | Genomic landmark | Assay ID |
|---|---|---|---|
rs2932538 | esv27061 | chr1:112,692,629-113,246,263 | Hs01327571 |
esv2757747* | chr1:113,157,135-116,741,372 | Hs01327571 | |
rs7129220 | nsv483076 | chr11:10,193,294-10,352,897 | Hs04399968 |
rs17608766 | dgv976e1 | chr17:44,083,914-45,277,333 | Hs00313538 |
esv2656635 | chr17:44,281,452-45,168,501 | Hs00313538 | |
nsv908562 | chr17:44,828,931-45,102,413 | Hs00313538 | |
dgv986e1 | chr17:44,971,360-45,277,333 | Hs00313538 | |
rs1327235 | dgv1306e1 | chr20:10,892,138-11,116,725 | Hs03126928 |