chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4179493216179493217GA47GENIChomozygous137280630
4179493528179493529TC50GENIChomozygous137280631
4179493726179493727CT57GENIChomozygous137280632
4179494427179494428AC65GENIChomozygous137280633
4179496113179496114CT25GENIChomozygous137280634
4179496374179496375AC45GENIChomozygous137280635
4179496780179496781CG54GENIChomozygous137280636
4179497153179497154TC41GENIChomozygous137280637
4179500319179500320GA48GENIChomozygous137280638
4179501662179501663GA39GENIChomozygous137280639
4179502830179502831CT50GENIChomozygous137280640
4179503221179503222TA47GENIChomozygous137280641
4179504579179504580GA39GENIChomozygous137280642
4179505536179505537AG53GENIChomozygous137280643
4179510429179510430GA57GENIChomozygous137280644
4179504839179504846TTTTTTG4GENICheterozygous136933114
4179504943179504944A17GENIChomozygous136933115