chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 69945451 69945452 A - 11 GENIC homozygous 698525010 14 69946916 69946917 A G 20 GENIC homozygous 547939340 14 69949045 69949046 C A 12 GENIC possibly homozygous 547939341 14 69951683 69951684 G GA 1 GENIC homozygous 698525011 14 69951754 69951755 A AGG 5 GENIC homozygous 698525012 14 69952415 69952416 T G 4 GENIC homozygous 547939342 14 69953756 69953757 A G 19 GENIC possibly homozygous 547939343 14 69954283 69954284 C T 5 GENIC homozygous 547939344 14 69955364 69955365 G T 12 GENIC possibly homozygous 547939345 14 69956318 69956319 A AGGT 7 GENIC possibly homozygous 698525013 14 69958117 69958118 A C 1 GENIC homozygous 547939346 14 69958963 69958964 C T 1 GENIC homozygous 547939347 14 69959664 69959665 A C 13 GENIC homozygous 547939348 14 69959966 69959967 C T 19 GENIC possibly homozygous 547939349 14 69961955 69961956 G A 17 GENIC homozygous 547939350 14 69962858 69962859 C T 2 GENIC homozygous 547939351 14 69970522 69970523 G A 20 GENIC possibly homozygous 547939352