chr start stop reference nuc variant nuc depth genic status zygosity variant ID 16 49282272 49282273 T C 30 GENIC homozygous 977264534 16 49285438 49285439 T C 29 GENIC homozygous 977264535 16 49297039 49297040 C G 18 GENIC homozygous 977264536 16 49297880 49297881 C G 34 GENIC homozygous 977264537 16 49297949 49297950 G A 32 GENIC homozygous 977264538 16 49298498 49298499 C G 26 GENIC homozygous 977264539 16 49305126 49305127 G C 13 GENIC homozygous 977264540 16 49310356 49310357 A G 21 GENIC homozygous 977264541 16 49313593 49313594 G A 27 GENIC homozygous 977264542 16 49316463 49316464 T C 30 GENIC homozygous 977264543 16 49319233 49319234 C T 34 GENIC homozygous 977264544 16 49321001 49321002 T C 46 GENIC homozygous 977264545 16 49321028 49321029 C T 43 GENIC homozygous 977264546 16 49322929 49322930 C T 12 GENIC homozygous 977264547 16 49323114 49323115 G A 22 GENIC homozygous 977264548 16 49323222 49323223 A T 18 GENIC homozygous 977264549 16 49323305 49323306 C T 36 GENIC homozygous 977264550 16 49325269 49325270 T C 18 GENIC homozygous 977264551 16 49325950 49325951 A G 19 GENIC homozygous 977264552 16 49326197 49326198 T C 25 GENIC homozygous 977264553