chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 2662678 2662679 T 27 GENIC homozygous 141675936 5 2662744 2662745 A G 24 GENIC possibly homozygous 141694817 5 2662812 2662813 G C 24 GENIC possibly homozygous 141694818 5 2662979 2662980 T C 29 GENIC homozygous 141694819 5 2663340 2663341 G C 26 GENIC homozygous 141694820 5 2666877 2666878 A G 32 GENIC homozygous 137359455 5 2667857 2667858 G A 21 GENIC homozygous 137359456 5 2670235 2670236 G A 31 GENIC homozygous 141694821 5 2671240 2671241 G A 37 GENIC homozygous 141694822 5 2671266 2671267 T A 34 GENIC homozygous 141694823 5 2671272 2671273 C A 36 GENIC homozygous 141694824 5 2671297 2671298 G A 30 GENIC homozygous 141694825 5 2671340 2671341 G A 34 GENIC homozygous 141694826 5 2671372 2671373 G A 30 GENIC homozygous 141694827 5 2671379 2671380 G A 31 GENIC homozygous 141694828 5 2671414 2671415 G A 34 GENIC homozygous 137359457 5 2672201 2672202 C T 28 GENIC homozygous 141694829 5 2672638 2672639 G A 36 GENIC homozygous 141694830 5 2672666 2672667 A G 35 GENIC homozygous 141694831 5 2674243 2674244 G A 44 GENIC homozygous 141694832 5 2674634 2674635 A G 32 GENIC homozygous 141694833 5 2676957 2676958 T C 35 GENIC homozygous 141694834