chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 17968143 17968144 G A 55 GENIC homozygous 796174020 17 17968418 17968419 C T 44 GENIC possibly homozygous 796174021 17 17970531 17970532 T C 43 GENIC possibly homozygous 796174022 17 17973250 17973251 A G 30 GENIC homozygous 796174023 17 17973650 17973651 C T 33 GENIC homozygous 796174024 17 17974779 17974780 T C 30 GENIC homozygous 796174025 17 17974868 17974869 A C 36 GENIC homozygous 796174026 17 17975208 17975209 A T 56 GENIC homozygous 796174027 17 17975962 17975963 C T 61 GENIC homozygous 796174028 17 17976744 17976745 C T 40 GENIC homozygous 796174029 17 17977294 17977295 G A 42 GENIC homozygous 796174030 17 17979545 17979546 G A 53 GENIC homozygous 796174031 17 17980422 17980423 A G 55 GENIC possibly homozygous 796174032 17 17980455 17980456 C T 66 GENIC homozygous 796174033 17 17981521 17981522 C T 49 GENIC possibly homozygous 796174034 17 17982574 17982575 A G 66 GENIC homozygous 796174035 17 17983069 17983070 A G 45 GENIC homozygous 796174036 17 17984201 17984202 A G 59 GENIC homozygous 796174037 17 17984402 17984403 G A 38 GENIC possibly homozygous 796174038 17 17984629 17984630 A T 69 GENIC possibly homozygous 796174039 17 17985000 17985001 G A 38 GENIC homozygous 796174040 17 17985691 17985692 A G 49 GENIC homozygous 796174041 17 17986707 17986708 C T 62 GENIC homozygous 796174042 17 17987759 17987760 G T 37 GENIC homozygous 796174043