chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221504177221504179GT--20GENIChomozygous61094030
1221504555221504556GA17GENIChomozygous61094031
1221505977221505978CT39GENICpossibly homozygous61094032
1221508190221508191CT49GENICpossibly homozygous61094033
1221509246221509247CT14GENIChomozygous61094034
1221510285221510286TA36GENIChomozygous61094036
1221511361221511362CCGTGT5GENIChomozygous61094038
1221511993221511994AG24GENIChomozygous61094039
1221513366221513367TC21GENIChomozygous61094040
1221514210221514211TC22GENIChomozygous61094041
1221515199221515200AG23GENIChomozygous61094042
1221515517221515518CT27GENIChomozygous61094043
1221515599221515600T-10GENICheterozygous62200202
1221515714221515718CTTT----3GENICheterozygous61094044
1221515714221515717CTT---3GENICheterozygous61094045