chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101410575314105754CT21GENICpossibly homozygous51622750
101410600514106006CA11GENIChomozygous51622751
101410891014108911CT4GENICheterozygous51622752
101410975114109752A-13GENIChomozygous51622756
101410989914109900GT11GENIChomozygous51622757