chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141712690117126902GC20GENIChomozygous48956376
141712725517127256AT30GENIChomozygous48547645
141712748317127484CT34GENIChomozygous48956378
141712763617127637CT17GENICpossibly homozygous48956380
141712769417127695TA24GENIChomozygous48547646
141712818817128189GC26GENIChomozygous48956382
141712856517128566GA20GENIChomozygous48956384
141712856717128568CT20GENIChomozygous48956386
141712864117128642AT26GENICpossibly homozygous48956388
141712880317128804CA26GENICpossibly homozygous48956390
141712890617128907GC20GENICpossibly homozygous48956392