chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
151821531218215313AC19GENIChomozygous139680089
151821580918215810GA17GENIChomozygous139680090
151821590018215901TC19GENIChomozygous139680091
151821605918216060CT28GENIChomozygous139680092
151821606418216065GA27GENIChomozygous139680093
151821612518216126GA24GENIChomozygous139680094
151821615618216157AG20GENIChomozygous139680095
151821692818216929CG20GENICpossibly homozygous139680096
151821702018217021GT16GENIChomozygous139680097
151821702118217022AC16GENIChomozygous139680098
151821704218217043GA19GENIChomozygous139680099
151821705618217057GA19GENIChomozygous139680100
151821798018217981CT21GENIChomozygous139680101
151821877818218779TG18GENIChomozygous139680102
151821979118219792AC7GENIChomozygous154933922
151822031518220316TC14GENIChomozygous139680103
151822089318220894GA25GENIChomozygous139680104
151822269818222699GA22GENIChomozygous139680105
151822436118224362TC21GENIChomozygous139680107
151822535218225353CT22GENIChomozygous139680109
151822539118225392CT24GENIChomozygous139680110
151822545218225453TC23GENIChomozygous139680111
151822588818225889GA13GENIChomozygous139680112
151822650218226503CA13GENIChomozygous139680116
151822663718226638TG17GENIChomozygous139680117
151822685518226856TC19GENIChomozygous139680118
151822696818226969GA25GENIChomozygous139680119
151822697018226971GA24GENIChomozygous139680120
151822731718227318AG14GENIChomozygous139680122
151822742918227430TC16GENIChomozygous139680124
151822664018226641G17GENIChomozygous139621083
151822861818228618ACGTGATG25GENIChomozygous146265758
151822140718221408A14GENIChomozygous139621081
151822370318223704A18GENIChomozygous139621082
151822734818227349CT13GENIChomozygous146271763