chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 40601461 40601462 C T 33 GENIC heterozygous 784534343 3 40601478 40601479 C T 33 GENIC heterozygous 784534344 3 40601496 40601497 G T 35 GENIC heterozygous 784534345 3 40601502 40601503 G A 34 GENIC heterozygous 784534346 3 40601505 40601506 C T 35 GENIC heterozygous 784534347 3 40601605 40601606 G T 29 GENIC heterozygous 784534348 3 40601607 40601608 T A 29 GENIC heterozygous 784534349 3 40601621 40601622 T C 34 GENIC heterozygous 784534350 3 40601624 40601625 G A 33 GENIC heterozygous 784534351 3 40601673 40601674 A G 39 GENIC heterozygous 784534352 3 40601852 40601853 C T 35 GENIC heterozygous 784534353 3 40601853 40601854 C G 35 GENIC heterozygous 784534354 3 40601907 40601908 T C 39 GENIC heterozygous 784534355 3 40601925 40601926 T C 44 GENIC heterozygous 784534356 3 40601946 40601947 G A 41 GENIC heterozygous 784534357 3 40601948 40601949 G A 41 GENIC heterozygous 784534358 3 40601961 40601962 T C 45 GENIC heterozygous 784534359 3 40601972 40601973 C T 46 GENIC heterozygous 784534360 3 40601977 40601978 A G 46 GENIC heterozygous 784534361 3 40601982 40601983 G A 43 GENIC heterozygous 784534362 3 40601993 40601994 T C 39 GENIC heterozygous 784534363 3 40601994 40601995 G A 40 GENIC heterozygous 784534364