chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 62071545 62071546 G C 31 GENIC homozygous 113830611 5 62071655 62071656 G C 22 GENIC possibly homozygous 113830613 5 62071857 62071858 G C 9 GENIC possibly homozygous 113830615 5 62072333 62072334 G C 4 GENIC homozygous 113830617 5 62073579 62073580 G T 24 GENIC homozygous 113830619 5 62074373 62074374 T C 33 GENIC homozygous 113830621 5 62076523 62076524 T C 39 GENIC homozygous 113830623 5 62079561 62079562 T C 10 GENIC possibly homozygous 113830625 5 62079573 62079574 T G 12 GENIC possibly homozygous 113830627 5 62079783 62079784 C T 36 GENIC homozygous 113830629 5 62081445 62081446 A G 28 GENIC homozygous 113830631 5 62082617 62082618 T C 14 GENIC homozygous 113830633 5 62088827 62088828 T A 57 GENIC homozygous 113830635 5 62090219 62090220 G A 52 GENIC possibly homozygous 113830637 5 62091563 62091564 T C 41 GENIC homozygous 113830639 5 62091945 62091946 C G 53 GENIC homozygous 113830641 5 62092493 62092494 G A 43 GENIC homozygous 113830643 5 62092706 62092707 T C 35 GENIC heterozygous 113830645 5 62093767 62093768 C T 51 GENIC possibly homozygous 113830647