chr start stop reference nuc variant nuc depth genic status zygosity variant ID 16 20370726 20370727 C T 49 GENIC possibly homozygous 782527510 16 20371702 20371703 G T 54 GENIC homozygous 782527511 16 20373814 20373815 C T 53 GENIC homozygous 782527512 16 20374276 20374277 A G 34 GENIC homozygous 782527513 16 20375359 20375360 C T 49 GENIC homozygous 782527514 16 20375440 20375441 T G 47 GENIC homozygous 782527515 16 20375700 20375701 C A 47 GENIC homozygous 782527516 16 20375702 20375703 G T 49 GENIC homozygous 782527517 16 20375827 20375828 A G 37 GENIC homozygous 782527518 16 20376160 20376161 T C 48 GENIC homozygous 782527519 16 20376386 20376387 A G 61 GENIC homozygous 782527520 16 20377069 20377070 G A 69 GENIC homozygous 782527521 16 20377227 20377228 T C 53 GENIC homozygous 782527522 16 20378173 20378174 G A 66 GENIC possibly homozygous 782527523 16 20379511 20379512 C T 49 GENIC homozygous 782527524