chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104501580745015808CT27GENIChomozygous51441582
104501714645017147TG24GENICpossibly homozygous51441584
104501742045017421GA18GENIChomozygous51441585
104502078345020784TC22GENIChomozygous51441587
104502187945021883TGTA----1GENIChomozygous51441588
104502219745022198TC15GENICheterozygous51441590
104502334645023347AAC8GENIChomozygous51441594
104502366345023664T-7GENIChomozygous51441595