chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5160425853160425854AG16GENICpossibly homozygous56359399
5160426593160426594TC10GENICpossibly homozygous56359401
5160426918160426919AG20GENICheterozygous56359403
5160428235160428236TC9GENIChomozygous56359407
5160428834160428835AC1GENIChomozygous57295000
5160430459160430460AG14GENIChomozygous57295009
5160430585160430586AG6GENIChomozygous56359413
5160431900160431901AG6GENICheterozygous57295012
5160431991160431992TC17GENIChomozygous56359417
5160432581160432582TC15GENIChomozygous56359419
5160432704160432705GA3GENICheterozygous57295015
5160432824160432825TA4GENICheterozygous57295018
5160433205160433206GGC19GENIChomozygous56359421
5160433988160433989AATGTGTGTG1GENIChomozygous56359423
5160434508160434509AATG4GENICheterozygous56359424
5160434566160434567GA11GENICpossibly homozygous57295021
5160435260160435261TA4GENIChomozygous57295024
5160435417160435418AC19GENICpossibly homozygous56359428
5160435627160435628TTC2GENICheterozygous57295027
5160435729160435730AT10GENIChomozygous57295030
5160436179160436180AG2GENIChomozygous57295033
5160437051160437052GA3GENIChomozygous57295036