chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 153555542 153555543 T G 23 GENIC homozygous 968532547 X 153598807 153598808 G A 23 GENIC homozygous 968532548 X 153598810 153598811 C A 22 GENIC homozygous 968532549 X 153598870 153598871 C A 28 GENIC homozygous 968532550 X 153602136 153602137 C T 26 GENIC homozygous 968532551 X 153602157 153602158 C T 23 GENIC homozygous 968532552 X 153602220 153602221 C T 20 GENIC homozygous 968532553 X 153640218 153640219 C T 26 GENIC homozygous 968532554 X 153692285 153692286 G C 19 GENIC possibly homozygous 968532555 X 153730942 153730943 T A 27 GENIC heterozygous 968532556 X 153772165 153772166 G T 38 GENIC homozygous 968532557 X 153836513 153836514 T G 24 GENIC homozygous 968532558