chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 110903046 110903047 A T 11 GENIC homozygous 992476334 X 110903049 110903050 T A 11 GENIC homozygous 992476335 X 110903269 110903270 G A 23 GENIC homozygous 992476336 X 110903511 110903512 G C 15 GENIC homozygous 992476337 X 110906891 110906892 C T 23 GENIC homozygous 992476338 X 110906892 110906893 C T 23 GENIC homozygous 992476339 X 110911116 110911117 C A 18 GENIC homozygous 992476340 X 110932836 110932837 G A 3 GENIC homozygous 992476341 X 110932839 110932840 C A 3 GENIC homozygous 992476342 X 110932845 110932846 C G 3 GENIC homozygous 992476343 X 110932849 110932850 C G 3 GENIC homozygous 992476344 X 110932855 110932856 C T 3 GENIC homozygous 992476345 X 110932864 110932865 A G 1 GENIC homozygous 992476346 X 110940136 110940137 G T 10 GENIC homozygous 992476347 X 110940211 110940212 G A 7 GENIC homozygous 992476348 X 110957382 110957383 T A 14 GENIC homozygous 992476349 X 110957386 110957387 A T 14 GENIC homozygous 992476350