chr start stop reference nuc variant nuc depth genic status zygosity variant ID 11 73124248 73124249 G A 14 GENIC homozygous 50830177 11 73125336 73125337 A T 18 GENIC homozygous 50830178 11 73125384 73125385 C - 10 GENIC possibly homozygous 50830179 11 73125454 73125455 T C 16 GENIC homozygous 50830180 11 73125558 73125559 A - 24 GENIC homozygous 50830181 11 73126003 73126004 T C 20 GENIC homozygous 50830182 11 73126671 73126672 G A 21 GENIC homozygous 50830183 11 73127223 73127224 C T 20 GENIC homozygous 50830184 11 73127553 73127554 T TA 15 GENIC homozygous 50830186 11 73128662 73128663 A C 31 GENIC homozygous 50830187 11 73128664 73128665 A G 31 GENIC homozygous 50830188 11 73129822 73129823 G A 17 GENIC homozygous 50830189 11 73131112 73131113 C T 14 GENIC homozygous 50830190 11 73131288 73131289 A ATCT 16 GENIC homozygous 50830191 11 73131328 73131329 G T 15 GENIC homozygous 50830192 11 73131597 73131602 GGTTC ----- 13 GENIC heterozygous 51295138 11 73131784 73131785 C G 14 GENIC homozygous 50830193 11 73133582 73133583 T C 21 GENIC homozygous 50830194 11 73134153 73134154 T C 16 GENIC homozygous 50830195