chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4181870484181870485GA16GENICpossibly homozygous501976650
4181871086181871087TC23GENIChomozygous501976651
4181871589181871590AG37GENIChomozygous501976652
4181871907181871908CT34GENICpossibly homozygous505535327
4181872014181872015CT31GENIChomozygous505535328
4181872168181872169GT22GENIChomozygous505535329
4181872359181872360TC15GENIChomozygous505535330
4181872420181872421A-12GENIChomozygous683847414
4181872427181872428A-13GENIChomozygous683847415
4181872443181872444A-7GENIChomozygous683847416