chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 98252938 98252939 C T 47 GENIC homozygous 110576374 2 98254532 98254533 C T 61 GENIC homozygous 110576376 2 98256127 98256128 A G 67 GENIC homozygous 110576378 2 98256316 98256317 T G 67 GENIC homozygous 110576380 2 98256331 98256332 T C 64 GENIC homozygous 109942031 2 98257993 98257994 A G 77 GENIC homozygous 109942037 2 98258299 98258300 C T 92 GENIC homozygous 109942039 2 98258462 98258463 G T 49 GENIC homozygous 109942041 2 98258480 98258481 G T 38 GENIC homozygous 110576382 2 98258494 98258495 C G 43 GENIC homozygous 109942043 2 98259703 98259704 C A 62 GENIC homozygous 109942047 2 98259783 98259784 A G 53 GENIC homozygous 109942049 2 98259804 98259805 A G 51 GENIC homozygous 109942051 2 98259809 98259810 T G 52 GENIC homozygous 109942053 2 98259818 98259819 A G 50 GENIC possibly homozygous 109942055 2 98259821 98259822 A G 51 GENIC homozygous 109942057 2 98259824 98259825 T G 51 GENIC homozygous 109942059 2 98259974 98259975 G A 59 GENIC homozygous 110576384 2 98260212 98260213 G A 63 GENIC homozygous 109942061 2 98260435 98260436 T C 65 GENIC homozygous 109942063 2 98261236 98261237 A G 70 GENIC homozygous 109942065 2 98261328 98261329 T G 73 GENIC possibly homozygous 109942067 2 98261917 98261918 A G 47 GENIC homozygous 109942069 2 98263010 98263011 C T 67 GENIC homozygous 109942073 2 98263131 98263132 C G 59 GENIC homozygous 109942075 2 98263246 98263247 C G 59 GENIC homozygous 109942077 2 98265723 98265724 G A 72 GENIC possibly homozygous 109942081 2 98266222 98266223 A T 75 GENIC homozygous 110576386 2 98266554 98266555 C G 55 GENIC homozygous 110576388 2 98266859 98266860 G A 63 GENIC possibly homozygous 110576390 2 98267645 98267646 C T 68 GENIC heterozygous 109942085 2 98268462 98268463 C T 62 GENIC homozygous 110576392