chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 153555542 153555543 T G 8 GENIC homozygous 974438660 X 153598807 153598808 G A 8 GENIC homozygous 974438661 X 153598810 153598811 C A 9 GENIC homozygous 974438662 X 153598870 153598871 C A 5 GENIC homozygous 974438663 X 153602136 153602137 C T 5 GENIC homozygous 974438664 X 153602157 153602158 C T 8 GENIC homozygous 974438665 X 153602220 153602221 C T 10 GENIC homozygous 974438666 X 153644852 153644853 T C 2 GENIC homozygous 974438667 X 153644858 153644859 T A 2 GENIC homozygous 974438668 X 153645152 153645153 T A 4 GENIC homozygous 974438669 X 153645153 153645154 T C 4 GENIC homozygous 974438670 X 153645194 153645195 G C 2 GENIC homozygous 974438671 X 153645339 153645340 A C 10 GENIC homozygous 974438672 X 153646501 153646502 G A 2 GENIC homozygous 974438673 X 153646502 153646503 A G 2 GENIC homozygous 974438674 X 153646535 153646536 G A 5 GENIC homozygous 974438675 X 153646544 153646545 G A 5 GENIC homozygous 974438676 X 153665740 153665741 A G 3 GENIC heterozygous 974438677 X 153692285 153692286 G C 6 GENIC homozygous 974438678 X 153730942 153730943 T A 14 GENIC heterozygous 974438679 X 153730959 153730960 G C 12 GENIC heterozygous 974438680 X 153730961 153730962 A G 13 GENIC heterozygous 974438681 X 153731007 153731008 T A 13 GENIC possibly homozygous 974438682 X 153772165 153772166 G T 8 GENIC homozygous 974438683 X 153836513 153836514 T G 4 GENIC homozygous 974438684