chr start stop reference nuc variant nuc depth genic status zygosity variant ID 16 49282272 49282273 T C 29 GENIC homozygous 956434702 16 49285438 49285439 T C 12 GENIC homozygous 956434703 16 49287269 49287270 C T 26 GENIC homozygous 956434704 16 49297039 49297040 C G 21 GENIC homozygous 956434705 16 49297880 49297881 C G 23 GENIC homozygous 956434706 16 49297949 49297950 G A 25 GENIC homozygous 956434707 16 49298498 49298499 C G 14 GENIC homozygous 956434708 16 49305126 49305127 G C 28 GENIC homozygous 956434709 16 49310356 49310357 A G 18 GENIC homozygous 956434710 16 49313593 49313594 G A 38 GENIC possibly homozygous 956434711 16 49316463 49316464 T C 12 GENIC homozygous 956434712 16 49319233 49319234 C T 33 GENIC homozygous 956434713 16 49321001 49321002 T C 43 GENIC homozygous 956434714 16 49321028 49321029 C T 42 GENIC homozygous 956434715 16 49322929 49322930 C T 23 GENIC homozygous 956434716 16 49323114 49323115 G A 38 GENIC homozygous 956434717 16 49323222 49323223 A T 29 GENIC homozygous 956434718 16 49323305 49323306 C T 18 GENIC homozygous 956434719 16 49325269 49325270 T C 26 GENIC homozygous 956434720 16 49325950 49325951 A G 46 GENIC homozygous 956434721 16 49326197 49326198 T C 32 GENIC homozygous 956434722 16 49328078 49328079 T C 27 GENIC homozygous 956434723