chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104526247945262480TG56GENIChomozygous51442115
104526273745262738CT29GENIChomozygous51442116
104526331645263317AG32GENIChomozygous51442117
104526501945265020AG44GENIChomozygous51442118
104526712545267128TTT---16GENIChomozygous51442120
104526714445267145TA20GENIChomozygous52317945
104526802045268021GA27GENIChomozygous51442121
104526727145267272CG24GENIChomozygous51636164
104526790745267908TC30GENIChomozygous51636165
104526936145269362AG15GENIChomozygous51442129
104526957945269580TA13GENIChomozygous51442130
104526969145269692CT45GENIChomozygous51636169
104527044945270450GA40GENIChomozygous51442131