chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 225521652 225521653 C T 17 GENIC homozygous 510479611 1 225521658 225521660 CA -- 11 GENIC possibly homozygous 685165074 1 225521659 225521661 AT -- 11 GENIC possibly homozygous 685165075 1 225521689 225521693 GTGC ---- 15 GENIC heterozygous 685165076 1 225521693 225521699 GTGTGT ------ 12 GENIC heterozygous 685165077 1 225521736 225521737 C CAA 17 GENIC homozygous 685165078 1 225521818 225521819 A - 38 GENIC homozygous 685165080 1 225521952 225521953 C T 42 GENIC homozygous 510479612 1 225522107 225522108 C CT 19 GENIC homozygous 685165081 1 225522446 225522447 G A 64 GENIC possibly homozygous 510479613 1 225522545 225522548 TGG --- 44 GENIC homozygous 685165082 1 225522654 225522655 G - 57 GENIC homozygous 685165083 1 225522827 225522828 C CATAT 53 GENIC homozygous 685165084 1 225523336 225523337 C T 60 GENIC homozygous 510479614 1 225523711 225523712 C T 59 GENIC homozygous 510479615 1 225523968 225523969 T A 61 GENIC homozygous 510479616 1 225524273 225524274 T G 55 GENIC homozygous 510479617 1 225524917 225524918 T C 68 GENIC homozygous 510479618 1 225525442 225525443 A G 63 GENIC homozygous 510479619