chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 30700624 30700625 T C 14 GENIC possibly homozygous 46704683 19 30705389 30705390 G A 12 GENIC possibly homozygous 46240571 19 30707003 30707005 AC -- 6 GENIC homozygous 46507548 19 30708395 30708396 T G 23 GENIC heterozygous 46704685 19 30714722 30714723 C T 4 GENIC homozygous 46704686 19 30714726 30714727 G GA 2 GENIC homozygous 46704687 19 30718070 30718071 T C 21 GENIC homozygous 46240574 19 30718499 30718500 G T 6 GENIC homozygous 46704690 19 30718970 30718971 C CAGG 6 GENIC homozygous 46487196 19 30719905 30719906 G A 18 GENIC possibly homozygous 46704691 19 30721273 30721274 T C 2 GENIC homozygous 46487202 19 30722593 30722594 C A 15 GENIC homozygous 46704692 19 30722784 30722785 A T 11 GENIC homozygous 46704693 19 30722891 30722892 G A 13 GENIC homozygous 46704694 19 30724343 30724344 T C 19 GENIC possibly homozygous 46240577 19 30725474 30725476 TC -- 22 GENIC homozygous 46704695