chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 227181388 227181389 A G 53 GENIC homozygous 110280064 2 227182141 227182142 G A 58 GENIC homozygous 111376335 2 227183806 227183807 T C 33 GENIC homozygous 110280070 2 227183810 227183811 T C 34 GENIC homozygous 110280072 2 227186932 227186933 C A 34 GENIC homozygous 111376336 2 227187706 227187707 T G 22 GENIC possibly homozygous 111376337 2 227189190 227189191 G A 52 GENIC possibly homozygous 111376338 2 227189294 227189295 C T 40 GENIC homozygous 111376339 2 227189609 227189610 T C 47 GENIC homozygous 111376340 2 227190380 227190381 A C 24 GENIC possibly homozygous 111376341 2 227191618 227191619 G A 48 GENIC homozygous 111376342 2 227193324 227193325 C T 39 GENIC homozygous 110280080 2 227195819 227195820 A G 50 GENIC homozygous 110280090 2 227196799 227196800 A G 49 GENIC heterozygous 111376343 2 227201727 227201728 A G 63 GENIC possibly homozygous 110280108 2 227202091 227202092 T C 55 GENIC homozygous 110280110 2 227203052 227203053 C T 36 GENIC homozygous 110280114 2 227204679 227204680 G A 46 GENIC homozygous 111376344 2 227205327 227205328 A G 63 GENIC homozygous 111376345