chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 150685448 150685449 T C 36 GENIC homozygous 979118225 5 150685716 150685717 T C 54 GENIC homozygous 979118226 5 150686020 150686021 G A 64 GENIC homozygous 979118227 5 150686369 150686370 C T 34 GENIC homozygous 979118228 5 150686423 150686424 T C 42 GENIC homozygous 979118229 5 150686627 150686628 G A 41 GENIC homozygous 979118230 5 150687272 150687273 C T 28 GENIC homozygous 979118231 5 150687321 150687322 G A 28 GENIC homozygous 979118232 5 150687870 150687871 T C 31 GENIC homozygous 979118233 5 150690906 150690907 T C 51 GENIC homozygous 979118234 5 150691762 150691763 G T 45 GENIC homozygous 979118235 5 150691895 150691896 C T 65 GENIC homozygous 979118236 5 150692007 150692008 G A 64 GENIC homozygous 979118237 5 150692098 150692099 G A 35 GENIC homozygous 979118238 5 150694736 150694737 T C 28 GENIC homozygous 979118239 5 150695315 150695316 C G 40 GENIC homozygous 979118240 5 150695753 150695754 G A 38 GENIC homozygous 979118241 5 150695760 150695761 C T 36 GENIC homozygous 979118242 5 150696514 150696515 C T 41 GENIC homozygous 979118243 5 150697024 150697025 C T 16 GENIC homozygous 979118244 5 150697094 150697095 C A 26 GENIC homozygous 979118245 5 150697095 150697096 A C 26 GENIC homozygous 979118246 5 150697188 150697189 T C 38 GENIC homozygous 979118247 5 150698126 150698127 C A 30 GENIC homozygous 979118248 5 150698211 150698212 G A 5 GENIC homozygous 979118249 5 150698221 150698222 C G 8 GENIC homozygous 979118250 5 150700013 150700014 G A 18 GENIC homozygous 979118251 5 150701466 150701467 T C 40 GENIC homozygous 979118252 5 150703071 150703072 A C 50 GENIC homozygous 979118253 5 150703412 150703413 T A 64 GENIC homozygous 979118254