chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
52623588826235889CT29GENICpossibly homozygous72137006
52623697026236971CT29GENIChomozygous72137010
52623715426237155AC34GENIChomozygous70322186
52623722526237226TC21GENIChomozygous70322188
52623767526237676CA30GENIChomozygous70322190
52623931526239316AC20GENIChomozygous70322192
52623955226239553CG24GENIChomozygous70322195
52623994926239950CT27GENIChomozygous70322197
52624008726240088CT17GENIChomozygous70322199
52624016826240169TC19GENIChomozygous70322201