chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106377610663776107GC44GENIChomozygous941772402
106377622363776224AG26GENIChomozygous941772403
106377820363778204CA23GENIChomozygous941772404
106378025263780253GT28GENIChomozygous941772405
106378119563781196CG21GENIChomozygous941772406
106378207463782075TC29GENIChomozygous941772407
106378294663782947CT30GENIChomozygous941772408
106378485563784856GA26GENIChomozygous941772409
106378928963789290TC30GENIChomozygous941772410
106378943963789440GT27GENIChomozygous941772411
106379056963790570AT7GENIChomozygous941772412
106379062063790621AC24GENIChomozygous941772413
106379067163790672TC33GENIChomozygous941772414
106379087663790877AG5GENIChomozygous941772415
106379279063792791CT26GENIChomozygous941772416
106379449263794493AC19GENIChomozygous941772417
106379466163794662GT25GENIChomozygous941772418
106379474163794742GC31GENIChomozygous941772419
106379501463795015TC35GENIChomozygous941772420