chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 154519443 154519444 A T 11 GENIC homozygous 975797096 5 154522676 154522677 C A 10 GENIC homozygous 975797097 5 154524077 154524078 A G 29 GENIC homozygous 975797098 5 154524810 154524811 T G 15 GENIC homozygous 975797099 5 154524824 154524825 A G 14 GENIC homozygous 975797100 5 154525219 154525220 T C 9 GENIC homozygous 975797101 5 154525514 154525515 C A 20 GENIC homozygous 975797102 5 154527506 154527507 C T 22 GENIC homozygous 975797103 5 154528250 154528251 T C 16 GENIC homozygous 975797104 5 154530266 154530267 A G 17 GENIC homozygous 975797105 5 154531151 154531152 G A 15 GENIC possibly homozygous 975797106 5 154531472 154531473 T C 10 GENIC homozygous 975797107 5 154531842 154531843 A C 16 GENIC homozygous 975797108 5 154531902 154531903 C A 10 GENIC homozygous 975797109 5 154531992 154531993 A T 15 GENIC homozygous 975797110 5 154532091 154532092 G A 13 GENIC homozygous 975797111 5 154533094 154533095 C T 20 GENIC homozygous 975797112 5 154533294 154533295 G A 13 GENIC homozygous 975797113 5 154533368 154533369 C T 13 GENIC homozygous 975797114 5 154533452 154533453 C T 11 GENIC homozygous 975797115 5 154533567 154533568 C T 16 GENIC homozygous 975797116 5 154533730 154533731 T C 14 GENIC homozygous 975797117 5 154533987 154533988 T C 11 GENIC homozygous 975797118 5 154534013 154534014 G C 15 GENIC homozygous 975797119 5 154535057 154535058 G T 27 GENIC homozygous 975797120 5 154535499 154535500 A G 32 GENIC homozygous 975797121 5 154537005 154537006 A G 11 GENIC homozygous 975797122 5 154537040 154537041 C G 7 GENIC homozygous 975797123 5 154538190 154538191 A G 11 GENIC homozygous 975797124 5 154538282 154538283 C G 13 GENIC homozygous 975797125 5 154538999 154539000 A G 25 GENIC homozygous 975797126 5 154539933 154539934 A G 10 GENIC homozygous 975797127 5 154540004 154540005 G A 6 GENIC homozygous 975797128 5 154540113 154540114 T G 17 GENIC homozygous 975797129