chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 93785877 93785878 G T 32 GENIC homozygous 994457115 9 93851508 93851509 C G 24 GENIC homozygous 994457116 9 93869876 93869877 A C 24 GENIC homozygous 994457117 9 93869877 93869878 A C 24 GENIC homozygous 994457118 9 93869882 93869883 A C 23 GENIC homozygous 994457119 9 93908262 93908263 T A 4 GENIC homozygous 994457120 9 93945469 93945470 A T 31 GENIC homozygous 994457121 9 93945481 93945482 C A 31 GENIC homozygous 994457122 9 93945535 93945536 T C 36 GENIC homozygous 994457123 9 93945547 93945548 G T 35 GENIC homozygous 994457124 9 93950044 93950045 T C 22 GENIC homozygous 994457125 9 93951104 93951105 T A 21 GENIC homozygous 994457126 9 93951105 93951106 C T 21 GENIC homozygous 994457127 9 93951489 93951490 T C 16 GENIC homozygous 994457128 9 93951668 93951669 G T 7 GENIC homozygous 994457129 9 93951669 93951670 C G 7 GENIC homozygous 994457130 9 93951690 93951691 C T 10 GENIC homozygous 994457131 9 93986952 93986953 C T 32 GENIC heterozygous 994457132 9 94017754 94017755 G A 19 GENIC possibly homozygous 994457133