chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10101872529101872530TTGA12GENICpossibly homozygous52514115
10101872529101872530TTGAGA12GENICheterozygous52969067
10101875230101875231AAT13GENIChomozygous51585831
10101876015101876016AAAG5GENIChomozygous52514117