chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1175444157175444158CT63GENIChomozygous108394111
1175444592175444593CT51GENICpossibly homozygous108394113
1175446633175446634GA42GENICpossibly homozygous108394115
1175446676175446677AG59GENIChomozygous108394117