chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 255382876 255382877 T C 20 GENIC possibly homozygous 668424827 1 255382893 255382894 A G 17 GENIC homozygous 668424828 1 255383559 255383560 C CCGTTA 8 GENIC homozygous 768139394 1 255383787 255383788 T C 19 GENIC possibly homozygous 668424829 1 255384349 255384350 C CCTT 4 GENIC heterozygous 768139395 1 255384674 255384675 T TA 10 GENIC homozygous 768139396 1 255386723 255386724 T C 26 GENIC possibly homozygous 668424830 1 255387328 255387329 C T 9 GENIC heterozygous 668424831 1 255387576 255387577 A G 15 GENIC homozygous 668424832 1 255387694 255387695 A G 9 GENIC possibly homozygous 668424833 1 255388344 255388345 A G 15 GENIC possibly homozygous 668424834 1 255388668 255388672 AAAC ---- 9 GENIC homozygous 768139397 1 255391173 255391174 G A 24 GENIC possibly homozygous 668424835 1 255391571 255391572 A G 20 GENIC homozygous 668424836 1 255391695 255391696 T C 17 GENIC possibly homozygous 668424837 1 255393301 255393302 A G 19 GENIC homozygous 668424838 1 255393392 255393393 T A 16 GENIC possibly homozygous 668424839 1 255393493 255393494 A AT 1 GENIC homozygous 768139398 1 255393562 255393563 T TGTAA 3 GENIC homozygous 768139399 1 255393574 255393575 T G 7 GENIC homozygous 668424840 1 255393970 255393971 T A 10 GENIC heterozygous 668424841 1 255394369 255394370 A C 2 GENIC homozygous 668424842 1 255395592 255395593 G A 25 GENIC possibly homozygous 668424843 1 255397033 255397034 C A 24 GENIC possibly homozygous 668424844 1 255397392 255397393 A G 19 GENIC possibly homozygous 668424845 1 255397632 255397633 C T 24 GENIC homozygous 668424846