chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 109972879 109972880 A T 2 GENIC homozygous 52331891 10 109972904 109972905 A G 6 GENIC homozygous 51600696 10 109973184 109973185 A G 16 GENIC possibly homozygous 51600697 10 109973262 109973263 T A 20 GENIC possibly homozygous 51600698 10 109973347 109973348 T C 20 GENIC homozygous 51600699 10 109973540 109973541 G A 22 GENIC homozygous 51600700 10 109974875 109974880 GTGTG ----- 12 GENIC heterozygous 51600701 10 109976102 109976103 G A 12 GENIC possibly homozygous 51600704 10 109976247 109976248 G C 7 GENIC homozygous 51600705 10 109976639 109976640 T C 10 GENIC heterozygous 51600710 10 109976655 109976656 C T 14 GENIC possibly homozygous 51600711 10 109976941 109976942 G A 23 GENIC possibly homozygous 51600712 10 109977462 109977463 G A 20 GENIC possibly homozygous 51600715 10 109977776 109977777 C T 12 GENIC homozygous 51600716 10 109978463 109978464 G A 30 GENIC possibly homozygous 51600717 10 109978962 109978963 C CA 6 GENIC heterozygous 51600718 10 109979045 109979046 A G 6 GENIC heterozygous 51600719 10 109979053 109979054 G GAACCC 4 GENIC heterozygous 51600720 10 109979055 109979056 T C 4 GENIC homozygous 52331893