chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 95390495 95390496 G GA 7 GENIC homozygous 51141204 13 95390496 95390497 G GAGAGAGAGAGAGA 7 GENIC homozygous 51141205 13 95390591 95390592 A G 25 GENIC possibly homozygous 50367456 13 95392130 95392131 T C 16 GENIC homozygous 50141341 13 95392212 95392213 C - 20 GENIC homozygous 50367467 13 95392668 95392669 T C 20 GENIC possibly homozygous 51141206 13 95393777 95393778 C T 14 GENIC possibly homozygous 50367469 13 95393913 95393914 G GT 7 GENIC heterozygous 50367473 13 95393930 95393931 C T 3 GENIC heterozygous 51141207 13 95394537 95394538 T C 33 GENIC homozygous 50141343 13 95394798 95394799 C A 9 GENIC homozygous 51141208 13 95395171 95395172 A G 26 GENIC homozygous 50141345 13 95395309 95395310 C T 19 GENIC heterozygous 50141347 13 95395630 95395631 G A 24 GENIC possibly homozygous 50141353 13 95395656 95395657 T TG 16 GENIC possibly homozygous 50141355 13 95395690 95395691 C T 11 GENIC possibly homozygous 51141209 13 95395923 95395924 T C 30 GENIC homozygous 50141357 13 95396618 95396619 C A 15 GENIC homozygous 50367481 13 95396657 95396664 TTTTTTT ------- 4 GENIC homozygous 51141210 13 95396678 95396679 T A 9 GENIC homozygous 51141211 13 95399578 95399579 C CT 26 GENIC possibly homozygous 51141212 13 95399929 95399930 C T 34 GENIC homozygous 51141213 13 95402988 95402989 C T 30 GENIC homozygous 51141214 13 95404646 95404647 T C 24 GENIC homozygous 50141368 13 95405541 95405542 C CTGTGTGTGTGTGTGTG 3 GENIC homozygous 50860568