chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 132824969 132824970 C T 17 GENIC possibly homozygous 630649152 3 132825168 132825169 A - 12 GENIC homozygous 745402762 3 132825181 132825182 C T 13 GENIC heterozygous 630649153 3 132825538 132825539 T C 18 GENIC homozygous 630649154 3 132825598 132825599 G A 11 GENIC homozygous 630649155 3 132825808 132825809 T C 24 GENIC possibly homozygous 630649156 3 132826043 132826044 C T 19 GENIC possibly homozygous 630649157 3 132826314 132826315 T C 22 GENIC homozygous 630649158 3 132826526 132826527 G GA 5 GENIC homozygous 745402763 3 132826563 132826564 T C 13 GENIC homozygous 630649159 3 132827011 132827012 C G 16 GENIC possibly homozygous 630649160 3 132827736 132827737 T TC 23 GENIC possibly homozygous 745402764 3 132827970 132827971 C G 22 GENIC possibly homozygous 630649161 3 132828273 132828274 A G 25 GENIC homozygous 630649162 3 132829043 132829044 T C 16 GENIC heterozygous 630649163 3 132829647 132829648 G GT 2 GENIC homozygous 745402766 3 132829725 132829726 A G 13 GENIC homozygous 630649164 3 132830845 132830846 G GA 4 GENIC heterozygous 745402767 3 132831972 132831973 G - 21 GENIC homozygous 745402768