chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 40695863 40695864 C T 16 GENIC homozygous 958965871 12 40696151 40696152 G A 30 GENIC homozygous 958965872 12 40696216 40696217 T C 27 GENIC homozygous 958965873 12 40696648 40696649 A T 15 GENIC homozygous 958965874 12 40696884 40696885 A T 13 GENIC homozygous 958965875 12 40697020 40697021 A C 15 GENIC possibly homozygous 958965876 12 40697446 40697447 T C 19 GENIC homozygous 958965877 12 40697467 40697468 C T 24 GENIC homozygous 958965878 12 40698282 40698283 C A 20 GENIC homozygous 958965879 12 40698935 40698936 A G 22 GENIC homozygous 958965880 12 40700586 40700587 T C 13 GENIC homozygous 958965881 12 40702959 40702960 T C 36 GENIC homozygous 958965882 12 40703828 40703829 C A 31 GENIC homozygous 958965883 12 40705325 40705326 A G 19 GENIC homozygous 958965884 12 40707476 40707477 C T 29 GENIC homozygous 958965885