chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3131501602131501634GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT--------------------------------1GENIChomozygous59047664
3131502722131502723AACTGT11GENICheterozygous57679430
3131502904131502905AG17GENICheterozygous60270723
3131503707131503708AT5GENICheterozygous60270724
3131503750131503751CG14GENICpossibly homozygous60270725
3131504168131504169TC11GENICpossibly homozygous60270726
3131504806131504807AG10GENICheterozygous57679433
3131504990131504991CT9GENICpossibly homozygous59701894
3131505682131505683AG20GENICpossibly homozygous58432520
3131506157131506158AT22GENICpossibly homozygous60270727
3131508800131508801CT20GENICpossibly homozygous60270728
3131514240131514241TC10GENIChomozygous60270729
3131516187131516188AG4GENICheterozygous57679457
3131521416131521417AT20GENICpossibly homozygous60270730