chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 172490279 172490280 A G 27 GENIC homozygous 975813574 5 172491197 172491198 C T 21 GENIC homozygous 975813575 5 172491314 172491315 C T 14 GENIC homozygous 975813576 5 172491996 172491997 T C 17 GENIC homozygous 975813577 5 172492247 172492248 T C 11 GENIC homozygous 975813578 5 172492253 172492254 C T 11 GENIC homozygous 975813579 5 172493271 172493272 C T 20 GENIC homozygous 975813580 5 172493291 172493292 G A 12 GENIC homozygous 975813581 5 172493570 172493571 G C 31 GENIC homozygous 975813582 5 172494808 172494809 T C 26 GENIC homozygous 975813583 5 172494883 172494884 C T 21 GENIC homozygous 975813584 5 172496684 172496685 C T 20 GENIC homozygous 975813585 5 172496946 172496947 T C 17 GENIC homozygous 975813586 5 172499650 172499651 G A 16 GENIC homozygous 975813587 5 172499683 172499684 A G 10 GENIC homozygous 975813588 5 172499955 172499956 C T 11 GENIC homozygous 975813589 5 172505834 172505835 G A 7 GENIC homozygous 975813590 5 172514486 172514487 G A 18 GENIC homozygous 975813591 5 172517554 172517555 C T 14 GENIC homozygous 975813592 5 172522126 172522127 A G 25 GENIC homozygous 975813593 5 172525073 172525074 T C 30 GENIC homozygous 975813594 5 172541982 172541983 A T 9 INTERGENIC homozygous 975813595