chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109094224190942245TGTG----9GENICpossibly homozygous51538760
109094615890946159TC49GENIChomozygous51538761
109094784590947846T-22GENIChomozygous51538762
109094785090947851T-25GENIChomozygous51538763
109094785390947854GC23GENIChomozygous51538764
109094786090947861TC25GENIChomozygous51538765
109094786290947863C-26GENIChomozygous51538766
109094786590947866CA24GENIChomozygous52397109
109094786890947869GGC24GENIChomozygous51538767
109094787390947874AG24GENIChomozygous51538768
109094787590947877TT--25GENIChomozygous51538769
109094788390947886TCC---25GENIChomozygous51538770
109094789390947894A-23GENIChomozygous51538771
109094789690947897CA23GENIChomozygous51997628
109095011290950113CCACACCACACACAACACACACAACACATAAACACATAAACACATACACACACCACACACACACACATAAACACACACAAACACACACCCACACACAACACATAAACACATACACACACCACACACACACA9GENICheterozygous52397113
109095014390950144A-12GENICheterozygous51738300
109095021090950211CCCA16GENICheterozygous51928350
109095022190950223CA--16GENICheterozygous52683515
109095093690950937TA29GENICheterozygous52323277
109095098090950981GGCA42GENICheterozygous51538778
109095364690953647AAACAC10GENIChomozygous51538780
109095721690957218AT--7GENIChomozygous51538781