chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108685435086854353GGG---34GENICpossibly homozygous51724240
108685539486855395GGA17GENIChomozygous51921698
108685550286855503CT26GENIChomozygous51921700
108685621286856213TG26GENIChomozygous51528996
108685678586856786AAC15GENICpossibly homozygous51921702
108685824786858248AC27GENIChomozygous51528999
108685881486858815GA33GENIChomozygous51921704
108685928786859288GC29GENIChomozygous51921706
108685945986859460AAC12GENIChomozygous51529001
108685958186859582TC24GENIChomozygous51724246
108686013286860133TG25GENIChomozygous51724250
108686132086861321GGCTCGTCCCCCTC11GENIChomozygous51724254
108686135986861360GT20GENIChomozygous51921708
108686208686862094TCCATCCA--------6GENIChomozygous51921710
108686209786862098AG22GENICheterozygous51921712