chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 153555542 153555543 T G 12 GENIC homozygous 951378410 X 153598807 153598808 G A 12 GENIC homozygous 951378411 X 153598810 153598811 C A 12 GENIC homozygous 951378412 X 153598870 153598871 C A 13 GENIC homozygous 951378413 X 153602136 153602137 C T 13 GENIC homozygous 951378414 X 153602157 153602158 C T 12 GENIC homozygous 951378415 X 153602220 153602221 C T 7 GENIC homozygous 951378416 X 153645059 153645060 T A 2 GENIC homozygous 951378417 X 153692285 153692286 G C 11 GENIC homozygous 951378418 X 153731007 153731008 T A 22 GENIC heterozygous 951378419 X 153772165 153772166 G T 7 GENIC homozygous 951378420 X 153836513 153836514 T G 15 GENIC homozygous 951378421