chr start stop reference nuc variant nuc depth genic status zygosity variant ID 16 49282272 49282273 T C 29 GENIC homozygous 881569675 16 49285438 49285439 T C 15 GENIC homozygous 881569676 16 49297039 49297040 C G 31 GENIC homozygous 881569677 16 49297880 49297881 C G 17 GENIC homozygous 881569678 16 49298498 49298499 C G 13 GENIC homozygous 881569679 16 49305126 49305127 G C 12 GENIC homozygous 881569680 16 49310356 49310357 A G 15 GENIC homozygous 881569681 16 49313593 49313594 G A 11 GENIC homozygous 881569682 16 49316463 49316464 T C 10 GENIC homozygous 881569683 16 49319233 49319234 C T 22 GENIC homozygous 881569684 16 49321001 49321002 T C 27 GENIC homozygous 881569685 16 49321028 49321029 C T 22 GENIC homozygous 881569686 16 49322867 49322868 G T 5 GENIC heterozygous 881569687 16 49322868 49322869 G T 5 GENIC heterozygous 881569688 16 49322929 49322930 C T 22 GENIC homozygous 881569689 16 49323222 49323223 A T 18 GENIC homozygous 881569690 16 49323305 49323306 C T 12 GENIC homozygous 881569691 16 49325269 49325270 T C 9 GENIC homozygous 881569692 16 49325950 49325951 A G 11 GENIC homozygous 881569693 16 49326197 49326198 T C 26 GENIC homozygous 881569694