chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 172490279 172490280 A G 31 GENIC homozygous 993829137 5 172491197 172491198 C T 21 GENIC possibly homozygous 993829138 5 172491314 172491315 C T 29 GENIC homozygous 993829139 5 172492247 172492248 T C 17 GENIC possibly homozygous 993829140 5 172492253 172492254 C T 19 GENIC possibly homozygous 993829141 5 172492753 172492754 A T 32 GENIC possibly homozygous 993829142 5 172493271 172493272 C T 34 GENIC possibly homozygous 993829143 5 172493291 172493292 G A 28 GENIC homozygous 993829144 5 172493570 172493571 G C 23 GENIC possibly homozygous 993829145 5 172494808 172494809 T C 37 GENIC homozygous 993829146 5 172494883 172494884 C T 47 GENIC homozygous 993829147 5 172496684 172496685 C T 26 GENIC possibly homozygous 993829148 5 172496946 172496947 T C 34 GENIC possibly homozygous 993829149 5 172497364 172497365 C T 16 GENIC homozygous 993829150 5 172499650 172499651 G A 27 GENIC possibly homozygous 993829151 5 172499683 172499684 A G 27 GENIC possibly homozygous 993829152 5 172499955 172499956 C T 28 GENIC possibly homozygous 993829153 5 172505834 172505835 G A 22 GENIC possibly homozygous 993829154 5 172514486 172514487 G A 29 GENIC homozygous 993829155 5 172517554 172517555 C T 43 GENIC homozygous 993829156 5 172522126 172522127 A G 25 GENIC homozygous 993829157 5 172525073 172525074 T C 28 GENIC homozygous 993829158