chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 124635881 124635882 G C 17 GENIC homozygous 984023459 X 124636223 124636224 G A 12 GENIC homozygous 984023460 X 124642122 124642123 A G 8 GENIC homozygous 984023461 X 124642452 124642453 A G 9 GENIC homozygous 984023462 X 124643201 124643202 C T 18 GENIC homozygous 984023463 X 124644532 124644533 C T 15 GENIC homozygous 984023464 X 124644755 124644756 C T 15 GENIC homozygous 984023465 X 124648028 124648029 G T 12 GENIC homozygous 984023466 X 124648043 124648044 C T 9 GENIC homozygous 984023467 X 124648547 124648548 A G 11 GENIC homozygous 984023468 X 124648836 124648837 T C 14 GENIC homozygous 984023469 X 124651865 124651866 G C 7 GENIC homozygous 984023470 X 124651980 124651981 C T 10 GENIC homozygous 984023471