chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 60619492 60619493 A G 28 GENIC homozygous 787520644 18 60619754 60619755 G T 19 GENIC possibly homozygous 787520645 18 60620465 60620466 T C 21 GENIC homozygous 787520646 18 60620560 60620561 G T 24 GENIC homozygous 787520647 18 60620603 60620604 T C 23 GENIC homozygous 787520648 18 60621069 60621070 G A 20 GENIC homozygous 787520649 18 60621383 60621384 T A 26 GENIC homozygous 787520650 18 60621387 60621388 A G 24 GENIC homozygous 787520651 18 60622829 60622830 T C 41 GENIC homozygous 787520652 18 60623204 60623205 C A 14 GENIC homozygous 787520653 18 60623296 60623297 T C 22 GENIC heterozygous 787520654 18 60625800 60625801 T C 16 GENIC homozygous 787520655 18 60626632 60626633 T C 20 GENIC homozygous 787520656 18 60627484 60627485 T C 20 GENIC homozygous 787520657 18 60628464 60628465 A C 21 GENIC homozygous 787520658 18 60628800 60628801 A G 23 GENIC homozygous 787520659