chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 120625392 120625393 G A 27 GENIC homozygous 108421285 X 120625488 120625489 T A 28 GENIC homozygous 108320557 X 120625906 120625907 G T 27 GENIC possibly homozygous 108421287 X 120626025 120626026 A C 24 GENIC homozygous 108421290 X 120626300 120626301 T C 22 GENIC homozygous 108421292 X 120627353 120627354 C G 30 GENIC homozygous 108421294 X 120628572 120628573 A T 30 GENIC homozygous 108421296 X 120629261 120629262 T G 24 GENIC homozygous 108421298 X 120629267 120629268 T G 23 GENIC homozygous 108421300 X 120630143 120630144 C T 24 GENIC homozygous 108421302 X 120630284 120630285 C A 29 GENIC homozygous 108421304 X 120630745 120630746 A C 29 GENIC homozygous 108421306 X 120630844 120630845 A G 28 GENIC homozygous 108421308 X 120631462 120631463 G A 23 GENIC homozygous 108421310 X 120631530 120631531 T C 23 GENIC homozygous 108421312 X 120632615 120632616 A G 17 GENIC homozygous 108421314 X 120633059 120633060 A G 20 GENIC homozygous 108421316 X 120633301 120633302 C T 22 GENIC homozygous 108421318 X 120634237 120634238 C A 20 GENIC homozygous 108421320 X 120634333 120634334 C T 28 GENIC homozygous 108421322 X 120636291 120636292 G A 20 GENIC homozygous 108421324 X 120637018 120637019 G C 22 GENIC homozygous 108421330 X 120636323 120636324 T A 28 GENIC homozygous 108421326 X 120636899 120636900 C A 21 GENIC homozygous 108421328 X 120637794 120637795 G A 33 GENIC homozygous 108421332 X 120637959 120637960 T C 17 GENIC homozygous 108421334 X 120640919 120640920 A G 22 GENIC homozygous 108421342 X 120638729 120638731 AA 22 GENIC homozygous 131243522 X 120639633 120639633 AAG 29 GENIC homozygous 131243523 X 120638350 120638351 A C 26 GENIC homozygous 108421336 X 120638623 120638624 T C 21 GENIC homozygous 108421338 X 120640193 120640194 A C 23 GENIC homozygous 108421340 X 120642747 120642747 A 18 GENIC homozygous 131243524 X 120647403 120647404 C A 23 GENIC homozygous 108421344 X 120644576 120644577 A T 22 GENIC homozygous 108454368