chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4142141866142141868AA--7GENICheterozygous57504024
4142141867142141868A-7GENICheterozygous56960102
4142142505142142506TC11GENIChomozygous57942208
4142143018142143019CT12GENIChomozygous57942210
4142143264142143265GC16GENIChomozygous57942213
4142144449142144450GA29GENIChomozygous57942216
4142146477142146478TC17GENIChomozygous57942222
4142149060142149061CG23GENIChomozygous57942224
4142150852142150853CA16GENIChomozygous57504048
4142151037142151038AC11GENIChomozygous57504050
4142151089142151090T-7GENICpossibly homozygous57942227
4142157157142157158TTC14GENIChomozygous56960107
4142157175142157176CCA14GENIChomozygous56960108
4142157481142157482CCT6GENICheterozygous58341684
4142157703142157704GGT21GENIChomozygous57942230
4142157757142157758CT13GENIChomozygous57942233
4142157831142157832TTA20GENIChomozygous57504064