chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 153555542 153555543 T G 22 GENIC homozygous 992496420 X 153598807 153598808 G A 16 GENIC homozygous 992496421 X 153598810 153598811 C A 16 GENIC homozygous 992496422 X 153598870 153598871 C A 21 GENIC homozygous 992496423 X 153602136 153602137 C T 21 GENIC homozygous 992496424 X 153602157 153602158 C T 18 GENIC homozygous 992496425 X 153602220 153602221 C T 16 GENIC homozygous 992496426 X 153692285 153692286 G C 17 GENIC homozygous 992496427 X 153755256 153755257 T G 13 GENIC homozygous 992496428 X 153755259 153755260 C T 13 GENIC homozygous 992496429 X 153755261 153755262 A T 13 GENIC homozygous 992496430 X 153763611 153763612 G C 3 GENIC homozygous 992496431 X 153763612 153763613 T C 3 GENIC homozygous 992496432 X 153772165 153772166 G T 28 GENIC homozygous 992496433 X 153915983 153915984 T C 7 GENIC homozygous 992496434 X 153915984 153915985 A T 7 GENIC homozygous 992496435