chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122752043127520432TTTCTCTC6GENIChomozygous50539719
122752111327521114T-4GENIChomozygous50154413
122752111627521117C-5GENIChomozygous50154415
122752112127521122GGA5GENIChomozygous50154417
122752112827521130CA--5GENIChomozygous50154419
122752114027521143CCA---4GENIChomozygous50154423
122752114727521148CCT6GENIChomozygous50154427
122752116227521163CCA6GENIChomozygous50154429
122752428327524284CCTT1GENIChomozygous50539720
122753111127531112TTTA14GENICheterozygous50827293
122753262427532625CCA5GENICheterozygous50154581
122753914127539142CCTT5GENICheterozygous50539732
122754104027541041C-1GENIChomozygous50154644
122754246327542464GT10GENIChomozygous50301983
122754246427542465AAATGTATGTATATCCATTATATATAGTATCTATACTATATATATGTATATATACATACACACATATCCAG10GENIChomozygous50539733
122755891527558916TTAGGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGG5GENIChomozygous50539735
122755967127559675TGTG----7GENIChomozygous50154662
122756088027560881CT14GENIChomozygous50485486
122756131927561320GGT10GENICheterozygous50406933
122756131927561320GGTTT10GENICpossibly homozygous50692805
122755829327558295GC--6GENICheterozygous50881309