chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7137072763137072764TG56GENICpossibly homozygous54253638
7137073166137073167TC50GENIChomozygous54137180
7137073935137073936CT63GENIChomozygous54137182
7137074229137074230GT50GENIChomozygous54137183
7137074980137074981AAC47GENIChomozygous54137185
7137074982137074983TTA45GENIChomozygous54137186
7137075455137075456CT37GENICpossibly homozygous54253640
7137075631137075636GATTA-----21GENIChomozygous54137187
7137075637137075638TC22GENICpossibly homozygous54137188
7137076074137076075C-29GENIChomozygous54137190