chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 2504901 2504902 T A 16 GENIC homozygous 53765669 7 2504988 2504989 C CTTT 3 GENIC homozygous 53765670 7 2505011 2505012 C T 11 GENIC heterozygous 54619412 7 2505756 2505757 A G 49 GENIC homozygous 53765671 7 2506481 2506482 A - 23 GENIC homozygous 53765673 7 2506517 2506518 C T 34 GENIC homozygous 53765674 7 2506687 2506688 G A 56 GENIC homozygous 53765675 7 2506709 2506713 GTGT ---- 33 GENIC homozygous 53765676 7 2506927 2506928 T TGACA 29 GENIC homozygous 53765677 7 2506928 2506929 C G 34 GENIC heterozygous 53765678 7 2507240 2507241 G GA 32 GENIC homozygous 53765679 7 2507310 2507311 G GTT 25 GENIC possibly homozygous 53765680 7 2509338 2509339 A C 41 GENIC homozygous 53765683 7 2510064 2510065 T G 24 GENIC heterozygous 53765684 7 2510372 2510373 A G 51 GENIC possibly homozygous 53765685 7 2511468 2511471 TTT --- 9 GENIC heterozygous 53765686 7 2511469 2511471 TT -- 9 GENIC possibly homozygous 53765687 7 2511487 2511488 G T 20 GENIC homozygous 53765688 7 2511616 2511617 T C 23 GENIC homozygous 53765690