chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 51225788 51225789 A G 23 GENIC homozygous 537280877 18 51226096 51226097 T C 37 GENIC homozygous 537280878 18 51227911 51227912 G T 26 GENIC homozygous 537280879 18 51227989 51227990 C CTTG 22 GENIC homozygous 698135913 18 51228306 51228307 T C 25 GENIC homozygous 540699341 18 51229836 51229837 T C 6 GENIC homozygous 540699342 18 51229985 51229986 T C 18 GENIC possibly homozygous 540699343 18 51230181 51230182 G A 16 GENIC homozygous 537280880 18 51230988 51230989 C T 38 GENIC homozygous 540699344 18 51233337 51233338 G C 30 GENIC homozygous 537280881 18 51234599 51234600 G A 31 GENIC homozygous 537280882 18 51235044 51235045 A G 43 GENIC homozygous 537280883 18 51235163 51235164 T C 37 GENIC homozygous 540699345 18 51236667 51236668 C A 12 GENIC homozygous 537280884 18 51237768 51237769 T A 1 GENIC homozygous 540699346 18 51237841 51237842 T C 4 GENIC heterozygous 540699347 18 51237841 51237842 T TATTC 4 GENIC homozygous 698135914 18 51238400 51238401 T C 26 GENIC homozygous 537280885 18 51239800 51239801 G GA 11 GENIC homozygous 698135915 18 51240151 51240152 T - 9 GENIC homozygous 698135917 18 51240961 51240962 A G 19 GENIC homozygous 537280886 18 51241908 51241909 A G 17 GENIC homozygous 537280887 18 51242025 51242026 G A 37 GENIC homozygous 537280888 18 51242209 51242210 A G 40 GENIC homozygous 537280889 18 51242388 51242389 C T 14 GENIC homozygous 537280890 18 51242608 51242609 A C 11 GENIC homozygous 537280891 18 51243135 51243136 T C 16 GENIC homozygous 537280892 18 51243389 51243390 G T 35 GENIC homozygous 540699348