chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 103975309 103975310 C G 2 GENIC homozygous 61733095 1 103975892 103975893 A AC 6 GENIC heterozygous 61733097 1 103976805 103976807 TG -- 10 GENIC homozygous 61733099 1 103977911 103977912 A G 7 GENIC possibly homozygous 61733101 1 103979378 103979379 G A 23 GENIC homozygous 61733109 1 103980780 103980781 C T 5 GENIC homozygous 61733110 1 103981157 103981158 T C 11 GENIC homozygous 61733112 1 103981201 103981202 C A 13 GENIC possibly homozygous 61733114 1 103981242 103981243 T C 5 GENIC homozygous 61733116 1 103981778 103981779 T G 3 GENIC homozygous 61733118 1 103981782 103981783 A C 2 GENIC homozygous 61733120 1 103981798 103981799 T - 3 GENIC homozygous 61733122 1 103981911 103981912 A G 2 GENIC homozygous 61733124 1 103982160 103982161 C T 14 GENIC possibly homozygous 61733126 1 103982675 103982676 G A 11 GENIC possibly homozygous 61733128 1 103983211 103983212 A T 13 GENIC homozygous 61733130 1 103983522 103983523 A G 23 GENIC possibly homozygous 61733132 1 103983926 103983929 AGG --- 11 GENIC homozygous 61733134