chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 81316390 81316391 G A 21 GENIC homozygous 111636450 3 81318164 81318165 G A 19 GENIC homozygous 111636451 3 81321725 81321726 T G 37 GENIC homozygous 111636452 3 81321942 81321943 A G 30 GENIC homozygous 111636453 3 81323305 81323306 G T 46 GENIC homozygous 111636454 3 81324148 81324149 A G 40 GENIC homozygous 111636455 3 81324452 81324453 A G 23 GENIC homozygous 111636456 3 81325052 81325053 T C 29 GENIC homozygous 111636457 3 81325108 81325109 A G 40 GENIC homozygous 111636458 3 81326916 81326917 G A 25 GENIC homozygous 111636459 3 81327297 81327298 G C 45 GENIC homozygous 111636460 3 81328295 81328296 A G 27 GENIC homozygous 111636461 3 81328566 81328567 C T 24 GENIC homozygous 111636463 3 81328778 81328779 C T 20 GENIC homozygous 111636464 3 81329624 81329625 A T 17 GENIC homozygous 111636466 3 81336318 81336319 G C 22 GENIC homozygous 111636467 3 81337289 81337290 T A 28 GENIC homozygous 111636469 3 81339700 81339701 T C 40 GENIC homozygous 111636470 3 81341735 81341736 G A 23 GENIC homozygous 111636472 3 81341885 81341886 C T 21 GENIC homozygous 111636473 3 81343462 81343463 A G 43 GENIC homozygous 111636474 3 81343485 81343486 A C 38 GENIC homozygous 111636475