chr start stop reference nuc variant nuc depth genic status zygosity variant ID 6 8003846 8003847 G A 30 GENIC homozygous 137718395 6 8158777 8158777 T 38 GENIC homozygous 137668424 6 8123191 8123195 CCTC 5 GENIC homozygous 141004888 6 8060431 8060432 G A 19 GENIC homozygous 147796671 6 8149604 8149605 T C 12 GENIC heterozygous 147796672 6 8065752 8065753 G C 28 GENIC possibly homozygous 140889073 6 8136449 8136450 A 34 GENIC possibly homozygous 137668418 6 8148058 8148059 G 8 GENIC homozygous 137668419 6 8151284 8151285 G 39 GENIC homozygous 137668420 6 8151703 8151705 CC 14 GENIC homozygous 137668421 6 8154484 8154484 G 31 GENIC homozygous 137668422 6 8157979 8157979 C 47 GENIC homozygous 137668423 6 8158788 8158789 G 37 GENIC homozygous 137668425 6 8158876 8158877 A 38 GENIC homozygous 137668429 6 8158803 8158804 T 40 GENIC homozygous 137668426 6 8158826 8158826 C 43 GENIC homozygous 137668427 6 8158860 8158860 G 39 GENIC homozygous 137668428 6 8160722 8160723 G 38 GENIC homozygous 137668430 6 8160761 8160761 C 35 GENIC homozygous 137668431 6 8160805 8160806 T 40 GENIC homozygous 137668432 6 8160814 8160815 C 40 GENIC homozygous 137668433 6 8161254 8161255 G 39 GENIC homozygous 137668434 6 8336778 8336780 AC 19 GENIC heterozygous 137668435 6 8385496 8385497 C 25 GENIC homozygous 137668436 6 8407291 8407292 C 14 GENIC heterozygous 141774372 6 8429050 8429051 C T 35 GENIC homozygous 137718397