chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 153555542 153555543 T G 24 GENIC homozygous 999153960 X 153598807 153598808 G A 11 GENIC homozygous 999153961 X 153598810 153598811 C A 11 GENIC homozygous 999153962 X 153598870 153598871 C A 11 GENIC homozygous 999153963 X 153602136 153602137 C T 11 GENIC homozygous 999153964 X 153602157 153602158 C T 14 GENIC homozygous 999153965 X 153602220 153602221 C T 11 GENIC homozygous 999153966 X 153624022 153624023 C T 17 GENIC homozygous 999153967 X 153645059 153645060 T A 8 GENIC homozygous 999153968 X 153645070 153645071 C A 10 GENIC homozygous 999153969 X 153692285 153692286 G C 8 GENIC homozygous 999153970 X 153730942 153730943 T A 20 GENIC heterozygous 999153971 X 153730959 153730960 G C 22 GENIC heterozygous 999153972 X 153730961 153730962 A G 22 GENIC heterozygous 999153973 X 153731007 153731008 T A 23 GENIC heterozygous 999153974 X 153772165 153772166 G T 22 GENIC homozygous 999153975 X 153836513 153836514 T G 13 GENIC homozygous 999153976