chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 41485285 41485286 G A 45 GENIC homozygous 139523741 14 41485297 41485298 G A 48 GENIC homozygous 139523742 14 41485597 41485598 A G 37 GENIC homozygous 139523743 14 41487009 41487010 A G 35 GENIC homozygous 139523749 14 41487401 41487402 A G 51 GENIC homozygous 139523752 14 41488702 41488703 T C 41 GENIC homozygous 139523756 14 41490074 41490075 T A 47 GENIC homozygous 139523761 14 41490084 41490084 CTA 45 GENIC homozygous 139395192 14 41486756 41486770 TTAACATATACCCA 48 GENIC homozygous 144941982 14 41487139 41487140 G 55 GENIC homozygous 144941983 14 41488649 41488649 GG 37 GENIC homozygous 139395191 14 41490808 41490809 G 42 GENIC homozygous 144941984 14 41490895 41490895 C 38 GENIC homozygous 139395193 14 41491918 41491919 C 30 GENIC homozygous 139395194 14 41492231 41492232 G A 48 GENIC homozygous 139523765 14 41493465 41493466 A C 40 GENIC homozygous 139523767 14 41495007 41495007 AC 26 GENIC possibly homozygous 144941985 14 41490214 41490215 G A 46 GENIC homozygous 144961687 14 41491755 41491756 C T 37 GENIC homozygous 144961688 14 41493799 41493800 C T 49 GENIC homozygous 144961689 14 41495053 41495054 C G 36 GENIC homozygous 144961690