chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 111735654 111735655 C T 9 GENIC homozygous 58175565 3 111735804 111735805 T C 15 GENIC homozygous 57988647 3 111735827 111735828 T G 10 GENIC homozygous 58175567 3 111735906 111735907 T A 13 GENIC homozygous 58175569 3 111736258 111736259 G A 14 GENIC homozygous 58175571 3 111736750 111736751 C CA 22 GENIC homozygous 57602900 3 111737037 111737038 G A 20 GENIC homozygous 58175573 3 111737191 111737192 G C 14 GENIC homozygous 57988650 3 111737599 111737600 C CT 9 GENIC homozygous 58175575 3 111737790 111737791 G A 12 GENIC homozygous 58175577 3 111739416 111739417 A G 18 GENIC homozygous 57988655 3 111739796 111739797 C T 15 GENIC homozygous 58175579 3 111740272 111740274 TC -- 12 GENIC homozygous 58175581 3 111740639 111740640 A C 20 GENIC homozygous 58175583 3 111740640 111740641 T C 20 GENIC homozygous 57988661 3 111741074 111741075 C T 16 GENIC homozygous 58175585 3 111741114 111741115 C CACTT 12 GENIC homozygous 57988664 3 111741259 111741260 A G 11 GENIC homozygous 57988667 3 111741585 111741586 T C 10 GENIC homozygous 58175587 3 111741761 111741762 G A 16 GENIC homozygous 58175589 3 111741865 111741866 A T 16 GENIC homozygous 58175591 3 111742340 111742341 C T 14 GENIC homozygous 58175595