chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 153555542 153555543 T G 10 GENIC homozygous 962806448 X 153598807 153598808 G A 15 GENIC homozygous 962806449 X 153598810 153598811 C A 14 GENIC homozygous 962806450 X 153598870 153598871 C A 13 GENIC homozygous 962806451 X 153602136 153602137 C T 15 GENIC homozygous 962806452 X 153602157 153602158 C T 16 GENIC homozygous 962806453 X 153602220 153602221 C T 10 GENIC homozygous 962806454 X 153692285 153692286 G C 13 GENIC possibly homozygous 962806455 X 153730959 153730960 G C 21 GENIC heterozygous 962806456 X 153730961 153730962 A G 21 GENIC heterozygous 962806457 X 153772165 153772166 G T 18 GENIC homozygous 962806458 X 153836513 153836514 T G 10 GENIC homozygous 962806459