chr start stop reference nuc variant nuc depth genic status zygosity variant ID 6 109216387 109216389 GT -- 21 GENIC possibly homozygous 727137322 6 109216449 109216450 A C 20 GENIC possibly homozygous 598311442 6 109216711 109216712 C G 9 GENIC homozygous 598311443 6 109217708 109217709 G A 15 GENIC homozygous 598311444 6 109218132 109218133 G A 5 GENIC homozygous 598311445 6 109218533 109218534 T C 10 GENIC homozygous 596421227 6 109218971 109218972 C G 19 GENIC homozygous 598311446 6 109219644 109219645 C G 3 GENIC homozygous 598311447 6 109219668 109219669 T C 4 GENIC homozygous 598311448 6 109219684 109219685 G GTCGTTTGGTCAGTTTC 1 GENIC homozygous 727137323 6 109219945 109219946 G A 28 GENIC homozygous 598311449 6 109220171 109220172 A G 14 GENIC possibly homozygous 596421228 6 109221203 109221204 T - 1 GENIC homozygous 727137324 6 109221479 109221480 A G 17 GENIC homozygous 596421229 6 109222377 109222378 T TTGTTTTATTTAATAACCCA 3 GENIC heterozygous 727137327 6 109225632 109225633 T C 20 GENIC homozygous 596421230 6 109225969 109225970 G C 12 GENIC heterozygous 596421231 6 109226303 109226304 G - 27 GENIC homozygous 727137328 6 109226869 109226870 T - 7 GENIC homozygous 727137329 6 109227301 109227302 C CTGTT 1 GENIC homozygous 727137331 6 109227384 109227385 T C 17 GENIC possibly homozygous 596421232 6 109227512 109227513 T A 16 GENIC homozygous 598311450 6 109228010 109228011 G A 19 GENIC possibly homozygous 598311451