chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104492716044927161AG38GENIChomozygous573508112
104493287844932897GCACCCCCTTCTCTCACAA-------------------19GENIChomozygous712959065
104493325544933256TC24GENICheterozygous573508113
104493325644933257CT24GENICheterozygous573508114
104493474744934748AAACACACACACAC13GENICpossibly homozygous712959070
104493527744935278AATGTGTGTGTGTGTGTG12GENICheterozygous712959073
104493527844935280TG--12GENICheterozygous712959071
104493614544936146GA26GENIChomozygous573508115
104493625244936253T-18GENIChomozygous712959074
104493741344937414TTACACACACACAC8GENICheterozygous712959076
104493741344937414TTACACACACACACAC8GENICpossibly homozygous712959077
104493825844938259AG6GENIChomozygous573508116
104493825944938260AG9GENIChomozygous573508117
104493829144938292CCT11GENIChomozygous712959078
104494024544940246CA25GENIChomozygous573508118
104494136044941361TC25GENIChomozygous573508119
104494158544941586AG24GENICpossibly homozygous573508120
104494200444942005GA22GENIChomozygous575269093
104494290544942906CT26GENIChomozygous573508121