chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 85130415 85130416 T C 86 GENIC homozygous 49020729 14 85131204 85131205 A G 44 GENIC possibly homozygous 49020730 14 85131228 85131229 C A 38 GENIC possibly homozygous 49020731 14 85131964 85131965 T - 53 GENIC homozygous 49020732 14 85132488 85132490 CT -- 55 GENIC homozygous 49020733 14 85134382 85134383 A G 61 GENIC homozygous 49020734 14 85135393 85135394 A C 52 GENIC homozygous 49020735 14 85135740 85135741 A G 50 GENIC possibly homozygous 49020736 14 85135881 85135883 TG -- 23 GENIC homozygous 49020737 14 85135923 85135924 T A 20 GENIC heterozygous 49020738 14 85135931 85135932 A T 19 GENIC possibly homozygous 49020739 14 85135950 85135951 T G 22 GENIC heterozygous 49020740 14 85136418 85136419 C T 38 GENIC homozygous 49020741 14 85136925 85136926 A AG 43 GENIC homozygous 49020742 14 85137230 85137231 A T 60 GENIC homozygous 49020743 14 85137602 85137603 T C 12 GENIC heterozygous 49020744 14 85138026 85138027 T C 70 GENIC homozygous 49020745 14 85138558 85138559 T C 66 GENIC homozygous 49020746 14 85138747 85138748 T C 57 GENIC heterozygous 49020747 14 85138755 85138756 C T 49 GENIC possibly homozygous 49020748 14 85138791 85138792 T A 53 GENIC homozygous 49020749 14 85138970 85138971 T - 22 GENIC homozygous 49020750 14 85139059 85139060 A AG 18 GENIC homozygous 49020751