chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1225334305225334306AT16GENICpossibly homozygous61600669
1225334422225334423CT4GENICheterozygous61926556
1225334850225334851AG22GENICpossibly homozygous61600671
1225334929225334930CT28GENICpossibly homozygous61926557
1225336120225336121TG14GENICheterozygous61600675
1225336158225336161GGG---1GENIChomozygous61926558
1225336714225336715TC8GENIChomozygous61101600
1225338635225338638TTT---2GENICheterozygous61926559
1225339093225339094AG24GENICpossibly homozygous61600697
1225339685225339686AG13GENIChomozygous61101611
1225340000225340001AG22GENICpossibly homozygous61600705
1225340596225340597A-2GENIChomozygous61101615
1225341238225341239TC13GENICheterozygous61600712
1225341902225341903CCA20GENIChomozygous61926560
1225343131225343132AG5GENIChomozygous61600718
1225343981225343982CA11GENIChomozygous61101619
1225336324225336327GGT---3GENIChomozygous62302589