chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 48741942 48741943 C T 9 GENIC possibly homozygous 46152033 19 48742300 48742301 C CCTGT 3 GENIC homozygous 46152034 19 48742496 48742497 T - 16 GENIC heterozygous 46152035 19 48743518 48743520 AG -- 12 GENIC homozygous 46152036 19 48744417 48744418 A G 12 GENIC homozygous 46152039 19 48744626 48744627 C T 3 GENIC homozygous 46152040 19 48746416 48746417 T A 14 GENIC possibly homozygous 46152046 19 48748913 48748914 A T 22 GENIC homozygous 46152048 19 48749139 48749140 C CT 2 GENIC heterozygous 46152049 19 48749331 48749332 C A 10 GENIC heterozygous 46152052 19 48749520 48749521 G A 10 GENIC homozygous 46152053 19 48749685 48749686 T C 1 GENIC homozygous 46152056 19 48749686 48749687 G C 1 GENIC homozygous 46152057 19 48749909 48749910 A - 4 GENIC heterozygous 46152058 19 48750282 48750283 G A 17 GENIC heterozygous 46152059 19 48750362 48750363 T G 19 GENIC possibly homozygous 46152060 19 48750935 48750936 T - 2 GENIC homozygous 46152061 19 48750975 48750976 C T 6 GENIC homozygous 46152062 19 48752741 48752742 T C 18 GENIC homozygous 46152066 19 48756999 48757000 A G 19 GENIC homozygous 46152076 19 48757139 48757140 A G 10 GENIC homozygous 46152077 19 48759185 48759186 G A 13 GENIC homozygous 46152081 19 48761460 48761461 T TCC 8 GENIC homozygous 46152082 19 48762353 48762354 A G 10 GENIC heterozygous 46152083 19 48763063 48763064 T - 3 GENIC homozygous 46152085 19 48764300 48764301 T C 14 GENIC homozygous 46152087 19 48765438 48765439 T TCTCTGGAGGC 5 GENIC homozygous 46152088 19 48766570 48766571 T C 13 GENIC possibly homozygous 46152089 19 48766964 48766965 C T 17 GENIC possibly homozygous 46152090 19 48767059 48767060 C T 12 GENIC heterozygous 46152091 19 48767483 48767484 C T 21 GENIC homozygous 46152092 19 48770546 48770547 A G 16 GENIC possibly homozygous 46152099