chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 130556123 130556124 A G 21 GENIC homozygous 115890580 7 130556165 130556166 C T 20 GENIC homozygous 115890582 7 130556669 130556670 A G 36 GENIC homozygous 115890584 7 130556712 130556713 G T 30 GENIC homozygous 115890586 7 130556727 130556728 A T 30 GENIC homozygous 115890588 7 130556738 130556739 A G 28 GENIC homozygous 115890590 7 130557064 130557065 T C 20 GENIC homozygous 115890592 7 130557291 130557292 G A 16 GENIC homozygous 115890594 7 130557836 130557837 C T 23 GENIC homozygous 115890596 7 130558518 130558519 G A 17 GENIC homozygous 115890598 7 130558657 130558658 T C 17 GENIC homozygous 115890600 7 130558747 130558748 G T 15 GENIC homozygous 115890602 7 130558847 130558848 T C 23 GENIC homozygous 115890604 7 130559154 130559155 T C 18 GENIC homozygous 115890606 7 130559962 130559963 A G 25 GENIC homozygous 115890608 7 130559993 130559994 C A 19 GENIC homozygous 115890609 7 130560530 130560531 A G 20 GENIC homozygous 115890611 7 130560735 130560736 G A 22 GENIC homozygous 115890613 7 130561146 130561147 A G 12 GENIC homozygous 115890615 7 130561201 130561202 C T 14 GENIC homozygous 115890617 7 130561298 130561299 G A 16 GENIC homozygous 115890619 7 130559385 130559386 G 9 GENIC homozygous 128520361 7 130559746 130559746 GA 25 GENIC homozygous 128520362 7 130561671 130561672 T C 18 GENIC homozygous 115890621 7 130561781 130561782 C T 16 GENIC homozygous 115890623 7 130561970 130561971 T C 15 GENIC homozygous 115890625 7 130563831 130563832 G C 29 GENIC homozygous 115890627 7 130564193 130564194 G C 17 GENIC homozygous 115890629 7 130564355 130564356 A T 23 GENIC homozygous 115890631 7 130564596 130564597 T C 15 GENIC homozygous 115890633 7 130564617 130564618 T C 12 GENIC homozygous 115890635