chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266928603266928604TC18GENIChomozygous108784286
1266928645266928646CT20GENIChomozygous108784287
1266928787266928788CT26GENIChomozygous109028558
1266928832266928833GA33GENIChomozygous108784288
1266929071266929072TC24GENIChomozygous108784289
1266929072266929073GA27GENIChomozygous108784290
1266929136266929137AG29GENIChomozygous108784291
1266929373266929374AG33GENIChomozygous108784293
1266929512266929513CT30GENIChomozygous108784294
1266929526266929527AC28GENIChomozygous108784295
1266930485266930486TC21GENIChomozygous108784296
1266930546266930547AG32GENIChomozygous108784297
1266930784266930785AG28GENIChomozygous108784298
1266931175266931176TC28GENIChomozygous108784299
1266930525266930526TC23GENIChomozygous108638820
1266931614266931615TC30GENICpossibly homozygous108638821
1266932396266932397GA39GENIChomozygous108638823
1266932399266932400CT34GENIChomozygous108638824
1266932408266932409CG31GENIChomozygous108638825
1266932413266932414TC27GENIChomozygous108638826
1266932420266932421AT25GENIChomozygous108638827
1266932561266932562AG33GENICheterozygous109028560
1266932441266932442TC34GENICpossibly homozygous108638829
1266932471266932472TA50GENICheterozygous108638830
1266932501266932502TA39GENICpossibly homozygous109028559
1266932913266932914AC30GENIChomozygous108638831
1266932929266932930TG28GENIChomozygous109028561
1266933417266933418GA39GENIChomozygous109028562
1266933543266933544TC35GENIChomozygous108638833
1266934167266934168TC35GENIChomozygous108638834
1266934856266934857CA24GENIChomozygous108638836
1266935538266935539CT29GENIChomozygous109028563