chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 19330513 19330514 A - 10 GENIC homozygous 50368645 12 19331155 19331156 G T 9 GENIC homozygous 50368651 12 19331356 19331357 A G 21 GENIC possibly homozygous 50368653 12 19331559 19331560 C T 14 GENIC possibly homozygous 50483076 12 19331634 19331635 T C 12 GENIC homozygous 50368655 12 19331771 19331772 T C 12 GENIC homozygous 50368657 12 19331990 19331991 T C 24 GENIC homozygous 50483078 12 19332106 19332107 T C 15 GENIC possibly homozygous 50368659 12 19333153 19333154 A G 6 GENIC heterozygous 50368663 12 19333235 19333236 T C 4 GENIC homozygous 50368665 12 19333328 19333329 T C 7 GENIC homozygous 50098673 12 19333952 19333953 C T 8 GENIC homozygous 50483080 12 19335028 19335029 T G 17 GENIC homozygous 50483088 12 19335702 19335703 A G 11 GENIC homozygous 50483090 12 19335795 19335796 A G 12 GENIC possibly homozygous 50368670 12 19336271 19336272 T C 24 GENIC possibly homozygous 50098683 12 19337560 19337564 GCCT ---- 1 GENIC homozygous 50098685 12 19337693 19337694 G A 4 GENIC homozygous 50483092 12 19337917 19337918 G A 13 GENIC possibly homozygous 50368674 12 19338889 19338890 C CTCTCCTT 1 GENIC homozygous 50536694 12 19338930 19338931 T C 14 GENIC homozygous 50098689 12 19340291 19340292 A G 16 GENIC possibly homozygous 50098699 12 19341298 19341299 A T 7 GENIC homozygous 50098701 12 19341300 19341301 T G 8 GENIC homozygous 50098703 12 19341477 19341478 A G 17 GENIC possibly homozygous 50098707 12 19342140 19342141 G A 2 GENIC homozygous 50483102 12 19342156 19342157 G - 6 GENIC heterozygous 50098715 12 19343288 19343289 C T 18 GENIC homozygous 50098719 12 19344414 19344415 G C 3 GENIC homozygous 50098721 12 19344497 19344498 T C 16 GENIC possibly homozygous 50098723 12 19344944 19344946 AC -- 9 GENIC possibly homozygous 50098727