chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 143134254 143134255 G GTACA 14 GENIC homozygous 691729711 X 143134364 143134365 C CA 13 GENIC homozygous 691729712 X 143134462 143134463 C G 10 GENIC homozygous 523068890 X 143134477 143134478 A G 13 GENIC homozygous 523068891 X 143134478 143134479 A G 16 GENIC homozygous 523068892 X 143134558 143134559 C T 32 GENIC homozygous 523068893 X 143134622 143134623 T A 15 GENIC homozygous 523068894 X 143134632 143134633 C - 11 GENIC heterozygous 691729713 X 143134636 143134637 G - 17 GENIC heterozygous 691729714 X 143152351 143152353 GT -- 13 GENIC heterozygous 691729715 X 143152365 143152367 GT -- 15 GENIC heterozygous 691729716 X 143162471 143162472 T - 29 GENIC homozygous 691729717 X 143163129 143163131 AC -- 22 GENIC homozygous 691729718 X 143164423 143164424 G - 12 GENIC homozygous 691729719 X 143164428 143164429 T TG 11 GENIC homozygous 691729720 X 143164433 143164434 T C 17 GENIC possibly homozygous 523068895 X 143164440 143164441 A - 14 GENIC homozygous 691729721 X 143164443 143164444 T C 17 GENIC homozygous 523068896 X 143164448 143164449 T C 19 GENIC homozygous 523068897 X 143164453 143164454 T - 15 GENIC homozygous 691729722 X 143164495 143164496 T TA 22 GENIC homozygous 691729723 X 143164499 143164500 A - 18 GENIC homozygous 691729724