chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191057729110577292TC47GENIChomozygous109634266
191057754810577549CT28GENIChomozygous109634268
191057831310578314CA49GENICpossibly homozygous109634270
191057849510578496GC43GENIChomozygous109634272
191057855310578554TA41GENICpossibly homozygous109634274
191057860810578609CG36GENIChomozygous109634276
191057928510579286TC38GENIChomozygous109634278
191057948510579486GT29GENIChomozygous109634280
191058155810581559CG33GENIChomozygous109634284
191057909710579098A47GENIChomozygous129583623
191058038010580380A40GENIChomozygous129583624
191058021710580218GA34GENIChomozygous109764606
191058073810580739TG25GENIChomozygous109956576