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Table 1 Humanin-like nuclear isoform gene chromosomal position (GRCh37)

From: Genetic variants in humanin nuclear isoform gene regions show no association with coronary artery disease

GeneChromosomePosition
MTRNR2L11722022437–22023991
MTRNR2L2579945819–79946854
MTRNR2L32055933496–55934878
MTRNR2L4163421053–3422283
MTRNR2L51057358750–57360488
MTRNR2L67142374131–142375525
MTRNR2L71037890366–37891859
MTRNR2L81110529434–10530723
MTRNR2L9662284008–62284534
MTRNR2L10X55207824–55208944
MTRNR2L111238107024–238108513
MTRNR2L12396336030–96337067
MTRNR2L134117220016–117221478