chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 153555542 153555543 T G 12 GENIC homozygous 971518313 X 153598611 153598612 T G 5 GENIC homozygous 971518314 X 153598612 153598613 C A 5 GENIC homozygous 971518315 X 153598653 153598654 G T 3 GENIC homozygous 971518316 X 153598681 153598682 G T 2 GENIC homozygous 971518317 X 153598870 153598871 C A 7 GENIC homozygous 971518318 X 153602136 153602137 C T 15 GENIC homozygous 971518319 X 153602157 153602158 C T 12 GENIC homozygous 971518320 X 153602220 153602221 C T 6 GENIC homozygous 971518321 X 153644980 153644981 G A 12 GENIC homozygous 971518322 X 153645059 153645060 T A 4 GENIC homozygous 971518323 X 153692285 153692286 G C 5 GENIC homozygous 971518324 X 153730959 153730960 G C 20 GENIC heterozygous 971518325 X 153730961 153730962 A G 20 GENIC heterozygous 971518326 X 153731007 153731008 T A 16 GENIC heterozygous 971518327 X 153772165 153772166 G T 6 GENIC homozygous 971518328 X 153808632 153808633 A G 10 GENIC heterozygous 971518329 X 153808638 153808639 C A 10 GENIC heterozygous 971518330 X 153836513 153836514 T G 5 GENIC homozygous 971518331