chr start stop reference nuc variant nuc depth genic status zygosity variant ID 6 93423066 93423067 G T 28 GENIC homozygous 798817851 6 93423898 93423899 G A 35 GENIC homozygous 798817852 6 93424917 93424918 C T 32 GENIC heterozygous 798817853 6 93425364 93425365 C T 40 GENIC homozygous 798817854 6 93432037 93432038 G A 25 GENIC homozygous 798817855 6 93432907 93432908 G A 37 GENIC homozygous 798817856 6 93433865 93433866 T A 30 GENIC homozygous 798817857 6 93436363 93436364 A T 29 GENIC possibly homozygous 798817858 6 93436454 93436455 G A 24 GENIC heterozygous 798817859 6 93436502 93436503 C T 21 GENIC possibly homozygous 798817860 6 93436504 93436505 G A 21 GENIC possibly homozygous 798817861 6 93436520 93436521 C T 24 GENIC possibly homozygous 798817862 6 93436543 93436544 G T 26 GENIC homozygous 798817863 6 93436549 93436550 C T 25 GENIC homozygous 798817864 6 93436589 93436590 C G 30 GENIC homozygous 798817865 6 93437053 93437054 G A 23 GENIC homozygous 798817866 6 93437242 93437243 G T 13 GENIC homozygous 798817867 6 93438052 93438053 C T 28 GENIC possibly homozygous 798817868 6 93440834 93440835 T C 42 GENIC heterozygous 798817869 6 93440867 93440868 A G 38 GENIC heterozygous 798817870 6 93440875 93440876 G T 39 GENIC heterozygous 798817871 6 93440923 93440924 A T 27 GENIC heterozygous 798817872 6 93441068 93441069 A C 44 GENIC heterozygous 798817873 6 93441365 93441366 C T 28 GENIC possibly homozygous 798817874