chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 53000668 53000668 G 18 GENIC homozygous 129053995 13 53000680 53000681 A 19 GENIC homozygous 129053996 13 53000684 53000684 TC 19 GENIC homozygous 129053997 13 53000687 53000687 C 22 GENIC homozygous 129053998 13 53000690 53000691 A 20 GENIC homozygous 129053999 13 53000692 53000692 TG 21 GENIC homozygous 129054000 13 53000695 53000695 G 22 GENIC homozygous 129054001 13 53000713 53000714 G 21 GENIC homozygous 129054002 13 53000720 53000721 A G 21 GENIC homozygous 118451067 13 53000736 53000736 C 20 GENIC homozygous 129054003 13 53000743 53000744 C T 21 GENIC homozygous 115010103 13 53000744 53000745 T C 21 GENIC homozygous 123735171 13 53000791 53000792 T 18 GENIC homozygous 129054004 13 53000911 53000911 T 9 GENIC homozygous 129054005 13 53000916 53000917 A C 10 GENIC homozygous 114550774 13 53000937 53000938 G 11 GENIC homozygous 129054006 13 53000957 53000957 A 14 GENIC homozygous 129054007 13 53000961 53000962 T 16 GENIC homozygous 129054008 13 53000977 53000977 T 18 GENIC homozygous 129054009 13 53000984 53000984 CC 19 GENIC homozygous 129054010 13 53001039 53001039 T 22 GENIC homozygous 129054015 13 53001016 53001016 T 19 GENIC homozygous 129054011 13 53001023 53001024 A 20 GENIC homozygous 129054012 13 53001026 53001027 G 21 GENIC homozygous 129054013 13 53001035 53001035 T 21 GENIC homozygous 129054014 13 53001028 53001029 G T 21 GENIC homozygous 114617580 13 53001040 53001040 T 22 GENIC homozygous 129054016 13 53001635 53001636 G T 1 GENIC homozygous 118451068 13 53001646 53001647 A T 1 GENIC homozygous 118451069 13 53003268 53003269 T C 11 GENIC homozygous 114346638 13 53003270 53003271 T G 10 GENIC homozygous 114346640 13 53003271 53003272 T G 10 GENIC homozygous 114346642 13 53003272 53003273 T G 10 GENIC homozygous 114346644 13 53020865 53020866 C A 7 GENIC homozygous 115067356