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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

Gene

Chromosome

Position

MTRNR2L1

17

22022437–22023991

MTRNR2L2

5

79945819–79946854

MTRNR2L3

20

55933496–55934878

MTRNR2L4

16

3421053–3422283

MTRNR2L5

10

57358750–57360488

MTRNR2L6

7

142374131–142375525

MTRNR2L7

10

37890366–37891859

MTRNR2L8

11

10529434–10530723

MTRNR2L9

6

62284008–62284534

MTRNR2L10

X

55207824–55208944

MTRNR2L11

1

238107024–238108513

MTRNR2L12

3

96336030–96337067

MTRNR2L13

4

117220016–117221478