chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108839420888394209GA59GENIChomozygous51729697
108839481088394811GC60GENICpossibly homozygous51729699
108839577488395775GGGTGT3GENICheterozygous51535181
108839691888396919GA61GENICpossibly homozygous51729701
108839792788397928GA52GENIChomozygous51729703
108839843988398440TA60GENIChomozygous51729705
108839898388398984AC58GENIChomozygous51729707
108839913188399132CT33GENICheterozygous51729709
108839942788399428CT34GENICpossibly homozygous51729711
108839943488399435TTA28GENIChomozygous51729713
108839998988399990AG41GENIChomozygous51729715
108840002688400027CA41GENICpossibly homozygous51535184
108840002988400030A-3GENIChomozygous51729717
108840025388400254TC61GENIChomozygous51729719
108840046988400470AG55GENIChomozygous51729721
108840048288400483GT54GENIChomozygous51729723
108840067788400678CT71GENICheterozygous51729725
108840068788400688AG76GENICheterozygous51729727
108840087588400876GA40GENIChomozygous51729729
108840096188400962T-38GENIChomozygous51729731
108840164588401646GA45GENIChomozygous51729733
108840178288401783GA62GENICpossibly homozygous51729734