chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144612923144612924TC40GENIChomozygous55763269
5144612986144612987CT26GENIChomozygous55763271
5144614198144614199CG26GENICpossibly homozygous55763273
5144614199144614200TC25GENICpossibly homozygous55763275
5144614219144614220CG9GENICheterozygous55763277
5144614345144614346GC18GENICheterozygous55763279
5144614787144614788TC6GENICheterozygous55763280
5144618219144618220GA35GENIChomozygous55763282
5144618530144618534AAAA----4GENIChomozygous55763284
5144621526144621527AT36GENIChomozygous55763286
5144622025144622026GGA11GENIChomozygous55763288
5144622902144622903CT48GENIChomozygous55763290
5144623071144623072TC43GENIChomozygous55763292
5144623265144623266TC38GENIChomozygous55763294
5144624113144624114G-24GENIChomozygous55763296
5144624236144624237CG46GENIChomozygous55763298
5144625373144625374AT36GENIChomozygous55763299