chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 59490763 59490764 A G 27 GENIC homozygous 969612322 5 59491034 59491035 G A 38 GENIC homozygous 969612323 5 59492252 59492253 G A 38 GENIC homozygous 969612324 5 59493293 59493294 T C 20 GENIC homozygous 969612325 5 59493344 59493345 C T 22 GENIC homozygous 969612326 5 59494021 59494022 G T 33 GENIC homozygous 969612327 5 59495021 59495022 A G 29 GENIC homozygous 969612328 5 59496242 59496243 A G 30 GENIC homozygous 969612329 5 59497270 59497271 G A 23 GENIC homozygous 969612330 5 59500179 59500180 A G 12 GENIC homozygous 969612331 5 59500828 59500829 G C 29 GENIC homozygous 969612332 5 59500873 59500874 G A 24 GENIC homozygous 969612333 5 59500875 59500876 C T 25 GENIC homozygous 969612334 5 59502207 59502208 C A 47 GENIC homozygous 969612335 5 59502243 59502244 C T 45 GENIC homozygous 969612336 5 59502300 59502301 G A 30 GENIC homozygous 969612337 5 59502340 59502341 C T 33 GENIC homozygous 969612338 5 59502468 59502469 C T 34 GENIC homozygous 969612339 5 59502683 59502684 T C 40 GENIC homozygous 969612340 5 59502698 59502699 A T 34 GENIC homozygous 969612341 5 59503232 59503233 C T 32 GENIC homozygous 969612342 5 59503245 59503246 C T 34 GENIC homozygous 969612343 5 59503453 59503454 C T 43 GENIC homozygous 969612344 5 59503514 59503515 T C 35 GENIC homozygous 969612345 5 59503720 59503721 T C 21 GENIC homozygous 969612346 5 59504116 59504117 T C 28 GENIC homozygous 969612347 5 59504488 59504489 A G 25 GENIC homozygous 969612348 5 59504888 59504889 T C 46 GENIC homozygous 969612349 5 59505140 59505141 C T 35 GENIC homozygous 969612350 5 59505463 59505464 T C 28 GENIC homozygous 969612351 5 59505718 59505719 G A 30 GENIC homozygous 969612352