chr start stop reference nuc variant nuc depth genic status zygosity variant ID 6 109215292 109215293 A G 10 GENIC heterozygous 579304084 6 109215591 109215592 G GT 13 GENIC homozygous 717700247 6 109215956 109215957 C T 21 GENIC homozygous 579304085 6 109216387 109216389 GT -- 18 GENIC possibly homozygous 717700248 6 109217437 109217438 G A 23 GENIC possibly homozygous 579304086 6 109218078 109218079 T G 1 GENIC homozygous 581314108 6 109218533 109218534 T C 15 GENIC possibly homozygous 579304087 6 109219644 109219645 C G 2 GENIC homozygous 581314109 6 109219668 109219669 T C 2 GENIC homozygous 581314110 6 109219684 109219685 G GTCGTTTGGTCAGTTTC 1 GENIC homozygous 717700249 6 109220171 109220172 A G 12 GENIC possibly homozygous 579304088 6 109220957 109220958 T - 6 GENIC homozygous 717700251 6 109220959 109220971 TATACATGTTAT ------------ 8 GENIC homozygous 717700252 6 109221479 109221480 A G 12 GENIC homozygous 579304089 6 109224503 109224504 C T 2 GENIC homozygous 579304090 6 109225632 109225633 T C 16 GENIC homozygous 579304091 6 109225969 109225970 G C 10 GENIC possibly homozygous 579304092 6 109226303 109226304 G - 14 GENIC homozygous 717700253 6 109226595 109226596 G A 23 GENIC possibly homozygous 579304093 6 109226868 109226869 C CT 8 GENIC heterozygous 717700255 6 109226869 109226870 T - 8 GENIC heterozygous 717700254 6 109227291 109227292 C CTGTTT 4 GENIC homozygous 717700256 6 109227384 109227385 T C 11 GENIC heterozygous 579304094 6 109227502 109227503 G A 13 GENIC homozygous 579304095 6 109227690 109227691 A T 13 GENIC homozygous 579304096 6 109227989 109227990 A G 10 GENIC possibly homozygous 579304097