chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 62122671 62122672 T TG 16 GENIC possibly homozygous 708450974 8 62122846 62122847 A AT 1 GENIC homozygous 708450975 8 62124790 62124791 T C 17 GENIC possibly homozygous 563846669 8 62125167 62125168 G T 6 GENIC homozygous 563846670 8 62125174 62125175 G GA 7 GENIC homozygous 708450976 8 62125724 62125725 T G 17 GENIC possibly homozygous 563846671 8 62126765 62126766 T C 19 GENIC homozygous 563846672 8 62127609 62127610 G A 27 GENIC possibly homozygous 563846673 8 62127639 62127640 C T 18 GENIC homozygous 565270358 8 62132718 62132719 C G 16 GENIC homozygous 565270359 8 62133017 62133018 C T 15 GENIC possibly homozygous 565270360 8 62133600 62133601 T A 6 GENIC homozygous 565270361 8 62134345 62134346 C T 17 GENIC heterozygous 565270362 8 62134519 62134520 C A 14 GENIC possibly homozygous 565270363 8 62136203 62136204 T C 14 GENIC homozygous 563846674 8 62137713 62137714 G A 27 GENIC homozygous 565270364 8 62138042 62138043 C T 24 GENIC homozygous 565270365 8 62140309 62140310 G A 9 GENIC possibly homozygous 565270366 8 62141096 62141097 C T 25 GENIC possibly homozygous 565270367 8 62142485 62142486 C G 16 GENIC homozygous 563846675 8 62142609 62142611 AG -- 16 GENIC heterozygous 708450977 8 62142641 62142642 A G 13 GENIC homozygous 565270368 8 62143432 62143433 A G 3 GENIC heterozygous 563846676 8 62144308 62144309 T C 24 GENIC possibly homozygous 563846677 8 62145559 62145560 C T 10 GENIC possibly homozygous 563846678 8 62145657 62145658 C T 17 GENIC possibly homozygous 565270369