chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
81297613812976139AG34GENIChomozygous117090120
81297618512976186CT39GENICpossibly homozygous117090121
81297755412977555GA23GENICpossibly homozygous117090122
81297786612977867CT25GENICpossibly homozygous117090123
81297829312978294AG22GENICpossibly homozygous117090124
81297962212979623AG23GENIChomozygous117090125
81297999812979999CT22GENIChomozygous117090126
81298068712980688GA35GENICpossibly homozygous117090127
81298226712982268CT47GENICpossibly homozygous117090129
81298417212984173GA22GENIChomozygous117090130
81299244212992443CT40GENIChomozygous117090142
81299286012992861GT24GENIChomozygous117090143
81299318112993182GA13GENICpossibly homozygous117090145