chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 60620465 60620466 T C 20 GENIC homozygous 956653931 18 60624918 60624919 A G 40 GENIC homozygous 956653932 18 60625800 60625801 T C 16 GENIC homozygous 956653933 18 60626632 60626633 T C 21 GENIC homozygous 956653934 18 60627484 60627485 T C 32 GENIC homozygous 956653935 18 60628219 60628220 G A 25 GENIC homozygous 956653936 18 60628292 60628293 G A 29 GENIC homozygous 956653937 18 60628800 60628801 A G 18 GENIC homozygous 956653938 18 60629023 60629024 T C 30 GENIC homozygous 956653939 18 60629052 60629053 C T 24 GENIC homozygous 956653940 18 60630749 60630750 A T 32 GENIC homozygous 956653941 18 60630945 60630946 C G 34 GENIC homozygous 956653942 18 60631097 60631098 C T 22 GENIC homozygous 956653943 18 60631478 60631479 C A 29 GENIC homozygous 956653944 18 60631670 60631671 A G 19 GENIC homozygous 956653945 18 60631920 60631921 G A 27 GENIC homozygous 956653946 18 60632136 60632137 C T 29 GENIC homozygous 956653947 18 60632157 60632158 G T 27 GENIC homozygous 956653948 18 60633665 60633666 G T 40 GENIC homozygous 956653949