chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 126196656 126196657 G A 34 GENIC homozygous 113996640 5 126198484 126198485 G T 26 GENIC homozygous 113996642 5 126198694 126198695 A G 37 GENIC homozygous 113996644 5 126200301 126200302 G A 5 GENIC homozygous 113996646 5 126200464 126200465 C A 30 GENIC homozygous 113996648 5 126205412 126205413 G A 29 GENIC possibly homozygous 113996650 5 126206686 126206687 A T 16 GENIC homozygous 113996652 5 126208062 126208063 C T 28 GENIC homozygous 113996654 5 126208247 126208248 G T 34 GENIC homozygous 113996656 5 126208411 126208412 G A 35 GENIC homozygous 113996658 5 126208590 126208591 T A 34 GENIC homozygous 113996660 5 126209139 126209140 G A 22 GENIC homozygous 113996662 5 126209608 126209609 A G 26 GENIC homozygous 113996664 5 126209611 126209612 G A 23 GENIC homozygous 113996666 5 126209705 126209706 T C 21 GENIC homozygous 113996668 5 126209708 126209709 G A 20 GENIC homozygous 113996670 5 126209715 126209716 G C 19 GENIC homozygous 113996672 5 126209768 126209769 C A 19 GENIC homozygous 113996674 5 126210065 126210066 T A 18 GENIC homozygous 113996675 5 126210514 126210515 A G 33 GENIC homozygous 113996677 5 126210631 126210632 T A 38 GENIC homozygous 113996679 5 126210873 126210874 T C 34 GENIC homozygous 113996681 5 126211601 126211602 C A 16 GENIC homozygous 113996683 5 126212657 126212658 C T 44 GENIC homozygous 113996685 5 126212671 126212672 A G 42 GENIC homozygous 113996687 5 126215100 126215101 G A 29 GENIC homozygous 113996689 5 126216747 126216748 C T 26 GENIC homozygous 113996691 5 126218232 126218233 C T 31 GENIC homozygous 113996693 5 126219108 126219109 A C 29 GENIC homozygous 113996695 5 126219778 126219779 T C 18 GENIC homozygous 113996697 5 126220467 126220468 A C 28 GENIC homozygous 113996701 5 126220266 126220267 C T 26 GENIC homozygous 113996699