chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 109972573 109972574 A AGTGTGTGTGTGTGT 8 GENIC heterozygous 52410206 10 109972573 109972574 A AGTGTGTGTGTGTGTGT 8 GENIC heterozygous 52410208 10 109972864 109972865 G GTT 10 GENIC heterozygous 52085308 10 109972864 109972865 G GTTT 10 GENIC heterozygous 52734752 10 109972879 109972880 A T 21 GENIC homozygous 52331891 10 109972904 109972905 A G 16 GENIC homozygous 51600696 10 109973184 109973185 A G 38 GENIC homozygous 51600697 10 109973262 109973263 T A 36 GENIC homozygous 51600698 10 109973347 109973348 T C 34 GENIC homozygous 51600699 10 109973540 109973541 G A 48 GENIC homozygous 51600700 10 109974875 109974880 GTGTG ----- 53 GENIC homozygous 51600701 10 109976102 109976103 G A 23 GENIC homozygous 51600704 10 109976247 109976248 G C 24 GENIC homozygous 51600705 10 109976371 109976372 G - 26 GENIC homozygous 51600706 10 109976380 109976387 TTGTTTG ------- 27 GENIC homozygous 51600708 10 109976639 109976640 T C 27 GENIC homozygous 51600710 10 109976655 109976656 C T 28 GENIC homozygous 51600711 10 109976941 109976942 G A 51 GENIC homozygous 51600712 10 109977040 109977044 CACA ---- 32 GENIC homozygous 51600713 10 109977462 109977463 G A 27 GENIC homozygous 51600715 10 109977776 109977777 C T 50 GENIC homozygous 51600716 10 109978463 109978464 G A 41 GENIC homozygous 51600717 10 109978962 109978963 C CA 30 GENIC possibly homozygous 51600718 10 109979045 109979046 A G 38 GENIC homozygous 51600719 10 109979053 109979054 G GAACCC 37 GENIC homozygous 51600720 10 109979055 109979056 T C 41 GENIC homozygous 52331893