chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 59491721 59491722 G A 9 GENIC homozygous 982163359 5 59492425 59492426 A G 7 GENIC homozygous 982163360 5 59493583 59493584 G A 20 GENIC homozygous 982163361 5 59496242 59496243 A G 23 GENIC homozygous 982163362 5 59497949 59497950 G A 17 GENIC homozygous 982163363 5 59502579 59502580 A C 20 GENIC homozygous 982163364 5 59502683 59502684 T C 29 GENIC homozygous 982163365 5 59502698 59502699 A T 30 GENIC homozygous 982163366 5 59502720 59502721 C T 29 GENIC homozygous 982163367 5 59502967 59502968 C T 20 GENIC homozygous 982163368 5 59503232 59503233 C T 14 GENIC homozygous 982163369 5 59503245 59503246 C T 13 GENIC homozygous 982163370 5 59503422 59503423 G A 10 GENIC homozygous 982163371 5 59503514 59503515 T C 9 GENIC homozygous 982163372 5 59504406 59504407 G A 19 GENIC homozygous 982163373 5 59504488 59504489 A G 14 GENIC homozygous 982163374 5 59504888 59504889 T C 31 GENIC homozygous 982163375 5 59504934 59504935 C T 19 GENIC homozygous 982163376 5 59505463 59505464 T C 25 GENIC homozygous 982163377 5 59505631 59505632 G C 11 GENIC homozygous 982163378 5 59508880 59508881 T C 13 GENIC homozygous 982163379