chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 15848683 15848684 T C 28 GENIC homozygous 45097676 X 15849513 15849514 G A 25 GENIC homozygous 45097677 X 15850273 15850287 ACACACACACACAC -------------- 8 GENIC homozygous 45501250 X 15850585 15850586 T TG 16 GENIC homozygous 45097678 X 15851377 15851378 T - 24 GENIC possibly homozygous 45097679 X 15854036 15854037 A G 21 GENIC homozygous 45097681 X 15856062 15856063 G GT 14 GENIC possibly homozygous 45097682 X 15858275 15858278 GTT --- 27 GENIC homozygous 45097684 X 15859016 15859019 CCT --- 4 GENIC heterozygous 45097687 X 15863490 15863491 T - 25 GENIC heterozygous 45097688 X 15863747 15863748 T - 31 GENIC homozygous 45097689 X 15865764 15865765 C A 31 GENIC homozygous 45097690 X 15866938 15866939 G GT 24 GENIC homozygous 45097691 X 15867080 15867081 G GTTTA 14 GENIC homozygous 45097692 X 15868475 15868476 A - 20 GENIC homozygous 45097693 X 15868484 15868485 T - 21 GENIC homozygous 45097694 X 15870864 15870865 T C 46 GENIC homozygous 45097695 X 15871410 15871411 G A 13 GENIC homozygous 45097696 X 15863489 15863491 TT -- 25 GENIC heterozygous 45252119