chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 48289683 48289684 G A 16 GENIC homozygous 800123785 13 48290572 48290573 C T 28 GENIC homozygous 800123786 13 48291011 48291012 A G 45 GENIC homozygous 800123787 13 48291308 48291309 A T 29 GENIC homozygous 800123788 13 48291450 48291451 C T 39 GENIC homozygous 800123789 13 48291571 48291572 T C 24 GENIC homozygous 800123790 13 48292967 48292968 T C 26 GENIC homozygous 800123791 13 48294043 48294044 G A 20 GENIC homozygous 800123792 13 48295128 48295129 G C 24 GENIC possibly homozygous 800123793 13 48295203 48295204 C G 10 GENIC possibly homozygous 800123794 13 48296042 48296043 T A 17 GENIC homozygous 800123795 13 48296242 48296243 T C 16 GENIC homozygous 800123796 13 48296271 48296272 G A 15 GENIC homozygous 800123797 13 48296275 48296276 T C 15 GENIC homozygous 800123798 13 48296328 48296329 G T 19 GENIC possibly homozygous 800123799 13 48296341 48296342 A G 6 GENIC homozygous 800123800 13 48296843 48296844 G A 29 GENIC homozygous 800123801 13 48297256 48297257 G T 25 GENIC homozygous 800123802 13 48297374 48297375 T C 23 GENIC homozygous 800123803