chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 121054275 121054276 A T 19 GENIC homozygous 125135004 X 121054857 121054858 C T 16 GENIC homozygous 125115151 X 121057928 121057929 T C 10 GENIC homozygous 125115155 X 121058116 121058117 A C 20 GENIC homozygous 125135007 X 121058356 121058357 C T 12 GENIC homozygous 125135008 X 121060019 121060020 G A 18 GENIC homozygous 125135009 X 121060318 121060319 T C 18 GENIC homozygous 125115157 X 121060578 121060579 A C 19 GENIC homozygous 125135010 X 121062270 121062271 T C 20 GENIC homozygous 125135011 X 121062757 121062758 A G 25 GENIC homozygous 125135012 X 121063889 121063890 C A 20 GENIC homozygous 125135013 X 121064459 121064460 G A 21 GENIC homozygous 125135015 X 121064510 121064511 C A 11 GENIC homozygous 125135016 X 121064761 121064762 A G 15 GENIC homozygous 125135017 X 121064774 121064775 A G 19 GENIC homozygous 125115159 X 121065191 121065192 G A 11 GENIC homozygous 125135018 X 121065397 121065398 T C 14 GENIC homozygous 125115160 X 121065614 121065615 G A 7 GENIC homozygous 125135019 X 121066142 121066143 G A 18 GENIC homozygous 125115161 X 121066214 121066215 C T 16 GENIC homozygous 125135020 X 121066305 121066306 A G 20 GENIC homozygous 125115162 X 121066516 121066517 T C 12 GENIC homozygous 125115164 X 121066522 121066523 G A 13 GENIC homozygous 125135021 X 121066619 121066620 C A 18 GENIC homozygous 125135022 X 121066670 121066671 G T 22 GENIC homozygous 125135023 X 121058802 121058803 G A 9 GENIC homozygous 125144356