chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 147501688 147501689 C T 18 GENIC homozygous 114046098 5 147501917 147501918 T C 18 GENIC homozygous 114046100 5 147502744 147502745 T C 23 GENIC homozygous 114046102 5 147504237 147504238 C T 15 GENIC homozygous 114046104 5 147507181 147507182 T G 10 GENIC homozygous 114046108 5 147507505 147507506 G T 9 GENIC homozygous 114046110 5 147510448 147510449 G A 24 GENIC homozygous 114046120 5 147511345 147511346 T C 21 GENIC homozygous 114046122 5 147514684 147514685 C T 23 GENIC homozygous 118846519 5 147514685 147514686 T C 24 GENIC homozygous 118846521 5 147519221 147519222 G T 4 GENIC homozygous 118943720 5 147519201 147519202 T A 2 GENIC homozygous 118943714 5 147519203 147519204 C A 2 GENIC homozygous 118943716 5 147519219 147519220 A C 4 GENIC homozygous 118943718 5 147527409 147527410 A G 2 GENIC homozygous 114046150 5 147531839 147531840 G T 20 GENIC homozygous 114046156 5 147534997 147534998 A G 30 GENIC homozygous 114046162