chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 51225788 51225789 A G 15 GENIC homozygous 528552087 18 51226096 51226097 T C 23 GENIC homozygous 528552088 18 51227911 51227912 G T 9 GENIC homozygous 528552089 18 51227989 51227990 C CTTG 10 GENIC homozygous 694862295 18 51228306 51228307 T C 12 GENIC homozygous 531826849 18 51229836 51229837 T C 16 GENIC homozygous 531826850 18 51229873 51229874 C CTTTATTTATTTA 7 GENIC homozygous 694862296 18 51229985 51229986 T C 17 GENIC homozygous 531826851 18 51230181 51230182 G A 14 GENIC homozygous 528552090 18 51230988 51230989 C T 6 GENIC homozygous 531826852 18 51233337 51233338 G C 14 GENIC homozygous 528552091 18 51234599 51234600 G A 15 GENIC homozygous 528552092 18 51235044 51235045 A G 19 GENIC homozygous 528552093 18 51235163 51235164 T C 16 GENIC homozygous 531826853 18 51236667 51236668 C A 19 GENIC homozygous 528552094 18 51237768 51237769 T A 19 GENIC homozygous 531826854 18 51237841 51237842 T TATTC 12 GENIC homozygous 694862297 18 51238400 51238401 T C 19 GENIC possibly homozygous 528552095 18 51239800 51239801 G GA 16 GENIC homozygous 694862298 18 51240150 51240152 TT -- 10 GENIC heterozygous 694862299 18 51240151 51240152 T - 10 GENIC heterozygous 694862300 18 51240961 51240962 A G 14 GENIC homozygous 528552096 18 51241908 51241909 A G 16 GENIC possibly homozygous 528552097 18 51242025 51242026 G A 22 GENIC homozygous 528552098 18 51242209 51242210 A G 13 GENIC homozygous 528552099 18 51242388 51242389 C T 19 GENIC homozygous 528552100 18 51242608 51242609 A C 22 GENIC homozygous 528552101 18 51243135 51243136 T C 18 GENIC homozygous 528552102 18 51243389 51243390 G T 32 GENIC homozygous 531826855