chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6115045146115045147TTTTCCA21GENIChomozygous54657025
6115046105115046106AG22GENIChomozygous54657027
6115046469115046470AC35GENIChomozygous54657029
6115046730115046731TTACCAATGCCTTCCTTCATA24GENIChomozygous55531482
6115046833115046834TC33GENIChomozygous54657035
6115046835115046836TA30GENIChomozygous54657037
6115047003115047005TT--19GENIChomozygous54657039
6115047396115047397CT25GENIChomozygous54657041
6115048071115048072AG23GENIChomozygous54657043
6115048337115048338AC35GENIChomozygous54657045
6115048749115048750AT43GENIChomozygous54657047
6115053567115053573GTGTGT------11GENIChomozygous55975920
6115054494115054495C-6GENIChomozygous54657049
6115054865115054870TTTTT-----6GENICheterozygous55726301
6115054868115054870TT--6GENICheterozygous55427606
6115056182115056183GA23GENIChomozygous54657056