chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 150637696 150637697 T C 28 GENIC homozygous 113182414 4 150638213 150638214 A G 27 GENIC homozygous 112884481 4 150638432 150638433 A G 32 GENIC homozygous 113182415 4 150638559 150638560 C T 21 GENIC homozygous 113182416 4 150639001 150639002 C T 26 GENIC homozygous 113182420 4 150639757 150639758 A G 37 GENIC homozygous 113182421 4 150640529 150640530 T G 28 GENIC homozygous 112884483 4 150640921 150640922 C T 20 GENIC possibly homozygous 112884485 4 150641793 150641794 C T 23 GENIC possibly homozygous 113182422 4 150642933 150642934 C A 47 GENIC homozygous 113182423 4 150643206 150643207 G T 34 GENIC homozygous 113182424 4 150643222 150643223 G A 29 GENIC homozygous 113182425 4 150643322 150643323 C T 22 GENIC homozygous 113182426 4 150643450 150643451 A T 35 GENIC homozygous 112884489 4 150643517 150643518 G A 31 GENIC homozygous 113182427 4 150643841 150643842 A C 35 GENIC homozygous 112884490 4 150643843 150643844 A G 35 GENIC homozygous 112884491 4 150643882 150643883 C T 39 GENIC homozygous 112884492 4 150643989 150643990 C T 38 GENIC homozygous 113182428 4 150644186 150644187 G A 21 GENIC homozygous 113182429 4 150644429 150644430 A G 32 GENIC homozygous 112884496 4 150644448 150644449 C T 35 GENIC homozygous 113182430 4 150644789 150644790 G A 20 GENIC homozygous 113182431 4 150645227 150645228 G A 35 GENIC homozygous 112884499 4 150645481 150645482 T C 24 GENIC homozygous 112884502