chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18118134281181343GA26GENIChomozygous642036225
18118192781181928AG29GENIChomozygous642036226
18118238681182387AG25GENIChomozygous642036227
18118277781182778TC26GENICpossibly homozygous642036228
18118402581184026CCAACA20GENIChomozygous752303305
18118458581184586TC22GENIChomozygous642036229
18118476681184767A-16GENIChomozygous752303306
18118486181184862TTA28GENIChomozygous752303308
18118489681184897T-24GENIChomozygous752303310
18118545681185458TT--25GENICpossibly homozygous752303311
18118545781185458T-25GENICheterozygous752303312
18118636281186363TG32GENIChomozygous642036230
18118681981186820AAT11GENIChomozygous752303313
18118694181186943GG--19GENIChomozygous752303314
18118714181187142AC13GENIChomozygous642036231
18118714281187143AT13GENIChomozygous642036232
18118714381187144AC12GENIChomozygous642036233
18118714881187149TTC8GENIChomozygous752303315
18118775781187758AG18GENICpossibly homozygous642036234
18118787381187874AG32GENIChomozygous642036235
18118801381188014GA28GENICpossibly homozygous642036236
18118818881188189CT30GENIChomozygous642036237
18118837581188376AC35GENICpossibly homozygous642036238
18118945681189457CT20GENICpossibly homozygous642036239
18118983081189831AG17GENIChomozygous642036240