chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5136708337136708338GA16GENIChomozygous114020580
5136709172136709173CT20GENIChomozygous114020582
5136710105136710106TC25GENIChomozygous114020584
5136710796136710797CT23GENIChomozygous114020586
5136710945136710946TC6GENIChomozygous114020588
5136711308136711309TG7GENIChomozygous114020590
5136712410136712411CT16GENIChomozygous114020592
5136713009136713010GC8GENICheterozygous114020593
5136713766136713767CT11GENIChomozygous114020595
5136713776136713777AG7GENIChomozygous114020597
5136713838136713839TA15GENICheterozygous114020599
5136714424136714425TA23GENICpossibly homozygous114020601
5136714843136714844TA22GENIChomozygous114020603