chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 104477431 104477432 G T 30 GENIC homozygous 971585614 1 104477450 104477451 G A 33 GENIC homozygous 971585615 1 104477451 104477452 A C 31 GENIC homozygous 971585616 1 104478219 104478220 C T 28 GENIC homozygous 971585617 1 104478304 104478305 C T 32 GENIC homozygous 971585618 1 104478470 104478471 G A 30 GENIC homozygous 971585619 1 104478570 104478571 G A 23 GENIC possibly homozygous 971585620 1 104478785 104478786 A G 22 GENIC homozygous 971585621 1 104478921 104478922 T C 27 GENIC homozygous 971585622 1 104479048 104479049 G C 31 GENIC possibly homozygous 971585623 1 104479358 104479359 T C 31 GENIC homozygous 971585624 1 104479677 104479678 C T 34 GENIC homozygous 971585625 1 104480400 104480401 G A 21 GENIC homozygous 971585626 1 104480826 104480827 A C 18 GENIC possibly homozygous 971585627 1 104480929 104480930 A G 27 GENIC homozygous 971585628 1 104481234 104481235 A G 20 GENIC homozygous 971585629