chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151012411151012412CA42GENIChomozygous114350443
5151013233151013234CT25GENIChomozygous114350445
5151013670151013671CT36GENIChomozygous114540871
5151013943151013944CT25GENICheterozygous114350447
5151014276151014277GC46GENIChomozygous114540873
5151015805151015806CT26GENIChomozygous114540875
5151016945151016946TC49GENICpossibly homozygous114350451
5151018404151018405AT25GENIChomozygous114350459
5151018479151018480GA23GENIChomozygous114540877
5151018541151018542TC19GENIChomozygous114350461
5151019126151019127AC50GENIChomozygous114350463
5151019527151019528AG21GENIChomozygous114540879
5151020116151020117AC35GENIChomozygous114350465
5151021666151021667GA32GENIChomozygous114350467
5151025211151025212AG38GENIChomozygous114350475
5151027655151027656TC23GENICpossibly homozygous114350477
5151017424151017425CT51GENICheterozygous114056557