chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 137126853 137126854 A C 19 GENIC homozygous 108243360 1 137126963 137126964 C T 38 GENIC homozygous 108243362 1 137127022 137127023 T G 37 GENIC homozygous 108243364 1 137128509 137128510 C T 12 GENIC heterozygous 108243371 1 137128827 137128828 A G 15 GENIC homozygous 108243373 1 137129176 137129177 T G 11 GENIC homozygous 108243377 1 137136358 137136359 G A 59 GENIC heterozygous 108743232 1 137136359 137136360 G A 59 GENIC heterozygous 109141856 1 137136362 137136363 T A 59 GENIC heterozygous 108243393 1 137136383 137136384 A G 57 GENIC heterozygous 109141862 1 137136394 137136395 G C 62 GENIC heterozygous 108743233 1 137136440 137136441 C A 62 GENIC heterozygous 109141864 1 137136467 137136468 A C 60 GENIC heterozygous 109141866 1 137136470 137136471 G C 62 GENIC heterozygous 109141868 1 137141106 137141107 G C 21 GENIC homozygous 108243405 1 137168090 137168091 T G 31 GENIC homozygous 108243458 1 137171305 137171306 C T 31 GENIC heterozygous 108243466 1 137238936 137238937 C T 6 GENIC homozygous 108243594 1 137238951 137238952 T G 3 GENIC homozygous 108743240 1 137238955 137238956 T G 2 GENIC homozygous 109326310 1 137238957 137238958 T G 2 GENIC homozygous 109326311 1 137238959 137238960 T A 2 GENIC homozygous 109326312