chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101410575314105754CT14GENIChomozygous51622750
101410600514106006CA8GENIChomozygous51622751
101410891014108911CT3GENICheterozygous51622752
101410965014109651A-1GENIChomozygous52646445
101410975114109752A-11GENIChomozygous51622756
101410989914109900GT9GENICpossibly homozygous51622757