chr start stop reference nuc variant nuc depth genic status zygosity variant ID 16 24863113 24863114 C CGT 21 GENIC homozygous 694742097 16 24863132 24863133 T A 23 GENIC homozygous 530868719 16 24863203 24863204 T A 24 GENIC homozygous 529781801 16 24863761 24863762 G A 13 GENIC homozygous 530868720 16 24863891 24863892 G C 17 GENIC homozygous 529781802 16 24863990 24863991 G GT 15 GENIC homozygous 694742098 16 24865275 24865276 A - 34 GENIC homozygous 694742099 16 24865616 24865617 C T 20 GENIC homozygous 529781803 16 24865676 24865677 T C 22 GENIC heterozygous 530868721 16 24866700 24866701 T C 13 GENIC homozygous 530868722 16 24866802 24866803 C T 16 GENIC possibly homozygous 530868723 16 24867027 24867028 C CT 30 GENIC homozygous 694742100 16 24867757 24867758 A G 24 GENIC homozygous 530868724 16 24868550 24868551 C T 29 GENIC homozygous 529781804 16 24869187 24869188 C T 13 GENIC homozygous 530868725 16 24869201 24869202 G A 13 GENIC homozygous 530868726 16 24869407 24869408 T A 16 GENIC homozygous 529781805 16 24869649 24869653 TAAG ---- 11 GENIC homozygous 694742101 16 24869717 24869718 G C 12 GENIC homozygous 530868727 16 24869748 24869749 A - 13 GENIC homozygous 694742102 16 24870274 24870275 C G 18 GENIC homozygous 530868728 16 24871355 24871356 C G 6 GENIC homozygous 529781806 16 24871565 24871566 T A 10 GENIC heterozygous 530868729 16 24871699 24871700 C T 12 GENIC heterozygous 530868730 16 24871737 24871738 C A 16 GENIC heterozygous 530868731 16 24871857 24871858 A C 10 GENIC heterozygous 530868732 16 24871867 24871868 C G 7 GENIC heterozygous 530868733