chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 69945451 69945452 A - 37 GENIC possibly homozygous 691366234 14 69946916 69946917 A G 48 GENIC homozygous 522722704 14 69949045 69949046 C A 42 GENIC homozygous 522722705 14 69951302 69951303 G C 46 GENIC possibly homozygous 522722706 14 69951683 69951684 G GA 32 GENIC heterozygous 691366235 14 69951754 69951755 A AGG 44 GENIC homozygous 691366236 14 69952415 69952416 T G 42 GENIC homozygous 522722707 14 69952520 69952521 G GAAA 36 GENIC homozygous 691366237 14 69952873 69952875 AA -- 15 GENIC homozygous 691366238 14 69953576 69953577 G - 21 GENIC homozygous 691366239 14 69953607 69953608 G A 27 GENIC possibly homozygous 522722708 14 69953611 69953612 G A 26 GENIC heterozygous 522722709 14 69953756 69953757 A G 39 GENIC homozygous 522722710 14 69954283 69954284 C T 56 GENIC homozygous 522722711 14 69955263 69955264 A AT 16 GENIC heterozygous 691366240 14 69955364 69955365 G T 38 GENIC homozygous 522722712 14 69956318 69956319 A AGGT 32 GENIC homozygous 691366242 14 69956535 69956536 A ACG 10 GENIC homozygous 691366243 14 69956537 69956538 A G 10 GENIC heterozygous 522722713 14 69956587 69956589 CG -- 1 GENIC homozygous 691366244 14 69956588 69956589 G - 1 GENIC homozygous 691366245 14 69956703 69956704 C T 30 GENIC homozygous 522722714 14 69958117 69958118 A C 59 GENIC possibly homozygous 522722715 14 69958963 69958964 C T 60 GENIC homozygous 522722716 14 69959664 69959665 A C 48 GENIC homozygous 522722717 14 69959966 69959967 C T 44 GENIC homozygous 522722718 14 69961955 69961956 G A 34 GENIC possibly homozygous 522722719 14 69962858 69962859 C T 63 GENIC homozygous 522722720 14 69967118 69967120 AA -- 32 GENIC possibly homozygous 691366246 14 69967119 69967120 A - 32 GENIC heterozygous 691366247 14 69969164 69969165 T TAAACAGTTAA 33 GENIC homozygous 691366248 14 69970522 69970523 G A 25 GENIC homozygous 522722721