chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 137651649 137651650 A G 23 GENIC homozygous 73078167 3 137651922 137651923 T C 29 GENIC homozygous 73078169 3 137652614 137652615 T A 33 GENIC homozygous 73078171 3 137652917 137652918 C T 36 GENIC homozygous 73078174 3 137653007 137653008 C A 29 GENIC homozygous 73078176 3 137653027 137653028 C T 28 GENIC homozygous 73078179 3 137653052 137653053 T C 33 GENIC homozygous 73078181 3 137653185 137653186 T C 21 GENIC homozygous 73078183 3 137653248 137653249 A G 25 GENIC homozygous 73078186 3 137653550 137653551 A G 29 GENIC homozygous 72500697 3 137653599 137653600 T G 29 GENIC homozygous 73078188 3 137653646 137653647 C T 28 GENIC homozygous 73078191 3 137653763 137653764 T C 36 GENIC homozygous 73078193 3 137653874 137653875 T A 30 GENIC homozygous 73078195 3 137653934 137653935 G A 30 GENIC homozygous 73078198 3 137654337 137654338 T C 20 GENIC homozygous 72500699 3 137654389 137654390 G A 19 GENIC possibly homozygous 73078200 3 137654437 137654438 G T 14 GENIC homozygous 73078203