chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 207964192 207964193 G A 29 GENIC homozygous 59356818 2 207968686 207968687 C CT 15 GENIC possibly homozygous 59356823 2 207969018 207969020 TT -- 11 GENIC heterozygous 59356824 2 207969019 207969020 T - 11 GENIC heterozygous 60514767 2 207970104 207970105 T TGTGC 31 GENIC homozygous 59356828 2 207970329 207970330 T - 9 GENIC heterozygous 59356829 2 207970759 207970760 C CAA 8 GENIC heterozygous 59356830 2 207970759 207970760 C CAAA 8 GENIC possibly homozygous 59356831 2 207973017 207973018 T C 30 GENIC homozygous 59356834 2 207973788 207973789 A C 22 GENIC homozygous 59931868 2 207975285 207975286 T C 33 GENIC homozygous 59931869 2 207976314 207976316 CA -- 3 GENIC homozygous 59931870 2 207976323 207976333 ACGCACGCAC ---------- 9 GENIC heterozygous 61659626 2 207977065 207977066 C T 21 GENIC homozygous 59931871 2 207977206 207977207 G A 24 GENIC homozygous 59931872 2 207977546 207977547 T C 12 GENIC homozygous 59931873 2 207977706 207977707 A G 23 GENIC homozygous 59931874 2 207978203 207978204 T - 17 GENIC homozygous 59931875 2 207978261 207978262 T - 15 GENIC possibly homozygous 59931876 2 207979027 207979028 A G 34 GENIC homozygous 59931877 2 207979187 207979188 A G 23 GENIC homozygous 59931878 2 207979227 207979228 A C 34 GENIC homozygous 59931879 2 207979259 207979260 G A 38 GENIC homozygous 59931880 2 207979291 207979292 C T 36 GENIC homozygous 59931881 2 207979456 207979457 T C 30 GENIC homozygous 59931882 2 207979618 207979619 A G 23 GENIC homozygous 59931883 2 207979674 207979675 T C 24 GENIC homozygous 59931884 2 207979864 207979865 G A 17 GENIC homozygous 59931885 2 207980879 207980880 G T 29 GENIC homozygous 59931886