chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 60619492 60619493 A G 35 GENIC possibly homozygous 777898842 18 60619754 60619755 G T 26 GENIC possibly homozygous 777898843 18 60620465 60620466 T C 64 GENIC homozygous 777898844 18 60620560 60620561 G T 51 GENIC homozygous 777898845 18 60620603 60620604 T C 51 GENIC homozygous 777898846 18 60621069 60621070 G A 47 GENIC homozygous 777898847 18 60621383 60621384 T A 45 GENIC homozygous 777898848 18 60621387 60621388 A G 42 GENIC homozygous 777898849 18 60622829 60622830 T C 37 GENIC homozygous 777898850 18 60623204 60623205 C A 42 GENIC homozygous 777898851 18 60623296 60623297 T C 42 GENIC heterozygous 777898852 18 60623305 60623306 C T 45 GENIC heterozygous 777898853 18 60625800 60625801 T C 32 GENIC homozygous 777898854 18 60626632 60626633 T C 24 GENIC homozygous 777898855 18 60627484 60627485 T C 61 GENIC homozygous 777898856 18 60628464 60628465 A C 71 GENIC homozygous 777898857 18 60628800 60628801 A G 50 GENIC homozygous 777898858