chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 153555542 153555543 T G 20 GENIC homozygous 948801635 X 153598807 153598808 G A 14 GENIC homozygous 948801636 X 153598810 153598811 C A 12 GENIC homozygous 948801637 X 153598870 153598871 C A 13 GENIC homozygous 948801638 X 153602136 153602137 C T 22 GENIC homozygous 948801639 X 153602157 153602158 C T 23 GENIC homozygous 948801640 X 153602220 153602221 C T 15 GENIC homozygous 948801641 X 153692285 153692286 G C 18 GENIC homozygous 948801642 X 153729685 153729686 A G 22 GENIC homozygous 948801643 X 153730942 153730943 T A 24 GENIC heterozygous 948801644 X 153730959 153730960 G C 21 GENIC heterozygous 948801645 X 153730961 153730962 A G 21 GENIC heterozygous 948801646 X 153731007 153731008 T A 20 GENIC heterozygous 948801647 X 153763611 153763612 G C 3 GENIC homozygous 948801648 X 153763612 153763613 T C 3 GENIC homozygous 948801649 X 153772165 153772166 G T 22 GENIC homozygous 948801650 X 153836513 153836514 T G 13 GENIC homozygous 948801651