chr start stop reference nuc variant nuc depth genic status zygosity variant ID 15 105400521 105400522 C T 15 GENIC homozygous 112635753 15 105400755 105400756 A C 22 GENIC homozygous 112635755 15 105404223 105404224 T C 35 GENIC homozygous 112635757 15 105406410 105406411 T C 20 GENIC homozygous 112635761 15 105406763 105406764 A G 12 GENIC homozygous 112767104 15 105407838 105407839 T C 29 GENIC homozygous 112635765 15 105407856 105407857 G T 28 GENIC homozygous 112635767 15 105410162 105410163 C A 20 GENIC homozygous 112635769 15 105410300 105410301 G T 28 GENIC homozygous 112635771 15 105410580 105410581 A G 18 GENIC homozygous 112635773 15 105410623 105410624 C T 18 GENIC homozygous 112635775 15 105411612 105411613 G A 16 GENIC homozygous 112635777 15 105412973 105412974 T C 22 GENIC homozygous 112635779 15 105413476 105413477 C A 24 GENIC homozygous 112635781 15 105413600 105413601 T C 20 GENIC possibly homozygous 112635783 15 105413663 105413664 G T 16 GENIC homozygous 112635785 15 105413770 105413771 A G 7 GENIC homozygous 112635787 15 105413893 105413894 A G 16 GENIC homozygous 112635789 15 105414590 105414591 A C 21 GENIC homozygous 112635791 15 105411575 105411576 T C 13 GENIC homozygous 112995263 15 105415291 105415292 T C 33 GENIC homozygous 112635793 15 105415688 105415689 C T 28 GENIC homozygous 112635795