chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 60619492 60619493 A G 20 GENIC homozygous 971284421 18 60620465 60620466 T C 29 GENIC homozygous 971284422 18 60620560 60620561 G T 40 GENIC homozygous 971284423 18 60620603 60620604 T C 32 GENIC homozygous 971284424 18 60621069 60621070 G A 29 GENIC homozygous 971284425 18 60621383 60621384 T A 34 GENIC homozygous 971284426 18 60621387 60621388 A G 33 GENIC homozygous 971284427 18 60622829 60622830 T C 26 GENIC homozygous 971284428 18 60623204 60623205 C A 22 GENIC homozygous 971284429 18 60625800 60625801 T C 25 GENIC homozygous 971284430 18 60626632 60626633 T C 28 GENIC homozygous 971284431 18 60627484 60627485 T C 30 GENIC homozygous 971284432 18 60628464 60628465 A C 32 GENIC homozygous 971284433 18 60628800 60628801 A G 25 GENIC homozygous 971284434