chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 71396571 71396572 G T 36 GENIC possibly homozygous 110396630 18 71397491 71397492 G T 34 GENIC possibly homozygous 110396632 18 71399316 71399317 G A 46 GENIC homozygous 110396634 18 71401711 71401712 T G 55 GENIC homozygous 110396636 18 71405662 71405663 A C 48 GENIC homozygous 110396638 18 71405783 71405784 A G 45 GENIC homozygous 110396640 18 71407029 71407030 C G 35 GENIC homozygous 110396642 18 71408209 71408210 A G 33 GENIC homozygous 110396644 18 71408365 71408366 T C 36 GENIC homozygous 110396646 18 71408716 71408717 C G 46 GENIC homozygous 110396648 18 71408768 71408769 A G 33 GENIC homozygous 110396650 18 71410217 71410218 A G 44 GENIC homozygous 110396652 18 71411191 71411192 T C 34 GENIC homozygous 110396655 18 71412021 71412022 C T 36 GENIC possibly homozygous 110396659 18 71412741 71412742 C T 48 GENIC possibly homozygous 110396661 18 71413136 71413137 G A 44 GENIC possibly homozygous 110396663 18 71413770 71413771 A G 57 GENIC homozygous 110396665 18 71415912 71415913 T C 32 GENIC homozygous 110396667 18 71415965 71415966 G C 36 GENIC possibly homozygous 110396669 18 71416628 71416629 G A 59 GENIC homozygous 110396671 18 71416943 71416944 T G 63 GENIC homozygous 110396673 18 71416972 71416973 C T 59 GENIC homozygous 110396675 18 71417634 71417635 A C 52 GENIC homozygous 110396677 18 71417713 71417714 G A 66 GENIC homozygous 110396679 18 71418082 71418083 T C 49 GENIC homozygous 110396681 18 71419044 71419045 A G 50 GENIC homozygous 110396683 18 71419130 71419131 T C 55 GENIC homozygous 110396685 18 71420413 71420414 G A 47 GENIC homozygous 110396687