chr start stop reference nuc variant nuc depth genic status zygosity variant ID 6 109216387 109216389 GT -- 13 GENIC possibly homozygous 745600885 6 109216449 109216450 A C 17 GENIC possibly homozygous 631267627 6 109216711 109216712 C G 16 GENIC homozygous 631267628 6 109217708 109217709 G A 22 GENIC possibly homozygous 631267629 6 109217869 109217870 C CTT 1 GENIC homozygous 745600887 6 109218132 109218133 G A 8 GENIC homozygous 631267630 6 109218533 109218534 T C 12 GENIC possibly homozygous 631267631 6 109218971 109218972 C G 26 GENIC possibly homozygous 631267632 6 109219644 109219645 C G 3 GENIC homozygous 631267633 6 109219668 109219669 T C 3 GENIC homozygous 631267634 6 109219945 109219946 G A 18 GENIC homozygous 631267635 6 109220171 109220172 A G 22 GENIC possibly homozygous 631267636 6 109221479 109221480 A G 15 GENIC possibly homozygous 631267637 6 109224251 109224252 C T 5 GENIC homozygous 631267638 6 109224503 109224504 C T 4 GENIC heterozygous 631267639 6 109225632 109225633 T C 22 GENIC homozygous 631267640 6 109225969 109225970 G C 12 GENIC heterozygous 631267641 6 109226303 109226304 G - 17 GENIC homozygous 745600891 6 109226869 109226870 T - 10 GENIC homozygous 745600892 6 109227301 109227302 C CTGTT 2 GENIC heterozygous 745600894 6 109227301 109227302 C CTGTTTGTTTGTT 2 GENIC heterozygous 745600895 6 109227384 109227385 T C 22 GENIC possibly homozygous 631267642 6 109227512 109227513 T A 24 GENIC homozygous 631267643 6 109228010 109228011 G A 19 GENIC possibly homozygous 631267644