chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 11627396 11627397 A C 10 GENIC heterozygous 53788708 7 11627487 11627488 G A 8 GENIC heterozygous 53788709 7 11628523 11628524 T C 10 GENIC heterozygous 53788710 7 11629634 11629635 A G 8 GENIC heterozygous 53788711 7 11630039 11630040 A C 5 GENIC heterozygous 53788713 7 11631838 11631839 C T 3 GENIC heterozygous 54181610 7 11632588 11632589 G A 14 GENIC homozygous 53788718 7 11633416 11633417 T C 21 GENIC homozygous 53788719 7 11633519 11633520 C A 2 GENIC homozygous 53788720 7 11633525 11633526 A G 4 GENIC heterozygous 53788721 7 11633538 11633539 A C 9 GENIC possibly homozygous 53788722 7 11634931 11634932 T C 6 GENIC homozygous 53788723 7 11635815 11635816 A T 9 GENIC possibly homozygous 53788724 7 11637249 11637250 T - 1 GENIC homozygous 54181611 7 11637433 11637434 A G 4 GENIC heterozygous 53788725 7 11639232 11639233 T C 6 GENIC heterozygous 53788726 7 11639499 11639500 C T 8 GENIC possibly homozygous 53788727 7 11639689 11639690 G A 14 GENIC possibly homozygous 53788728 7 11639873 11639874 A AT 14 GENIC homozygous 53788729 7 11640906 11640907 T C 6 GENIC homozygous 54884856 7 11640907 11640908 C A 7 GENIC homozygous 54181612 7 11642750 11642751 A G 6 GENIC heterozygous 53788731 7 11643494 11643495 A G 19 GENIC homozygous 53788732 7 11643826 11643827 T TCTGG 4 GENIC homozygous 53788733 7 11643835 11643836 C T 7 GENIC possibly homozygous 53788734 7 11644484 11644485 T G 13 GENIC possibly homozygous 53788736 7 11644524 11644525 T C 21 GENIC homozygous 53788737 7 11644756 11644757 T C 13 GENIC homozygous 53788738 7 11645636 11645637 C T 2 GENIC homozygous 53788739