chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 17966664 17966665 C T 12 GENIC homozygous 974069542 17 17966674 17966675 T C 11 GENIC heterozygous 974069543 17 17968143 17968144 G A 34 GENIC homozygous 974069544 17 17968418 17968419 C T 12 GENIC homozygous 974069545 17 17970531 17970532 T C 11 GENIC homozygous 974069546 17 17973250 17973251 A G 23 GENIC homozygous 974069547 17 17974779 17974780 T C 13 GENIC homozygous 974069548 17 17974868 17974869 A C 14 GENIC homozygous 974069549 17 17975208 17975209 A T 13 GENIC homozygous 974069550 17 17975962 17975963 C T 24 GENIC homozygous 974069551 17 17976532 17976533 A T 23 GENIC homozygous 974069552 17 17976744 17976745 C T 18 GENIC homozygous 974069553 17 17977294 17977295 G A 20 GENIC homozygous 974069554 17 17979545 17979546 G A 20 GENIC homozygous 974069555 17 17980422 17980423 A G 20 GENIC homozygous 974069556 17 17980455 17980456 C T 21 GENIC homozygous 974069557 17 17980654 17980655 T G 18 GENIC homozygous 974069558 17 17981521 17981522 C T 13 GENIC homozygous 974069559 17 17983069 17983070 A G 13 GENIC homozygous 974069560 17 17984402 17984403 G A 26 GENIC homozygous 974069561 17 17984629 17984630 A T 11 GENIC homozygous 974069562 17 17985000 17985001 G A 23 GENIC homozygous 974069563 17 17985691 17985692 A G 8 GENIC homozygous 974069564 17 17986707 17986708 C T 18 GENIC possibly homozygous 974069565