chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108506456885064569AG10GENIChomozygous51525084
108506593585065936CT18GENIChomozygous53160193
108506640085066401AG17GENIChomozygous53160195
108506863285068633TC13GENIChomozygous53160197
108506907085069071AG25GENIChomozygous51525088
108506925785069260TCG---18GENIChomozygous53160199
108507039485070395A-25GENICpossibly homozygous51525091
108507163585071695CCCAGCCCCAGCCCCAGCCCCAGCCCCAGCCCCAGCCCCAGCCCCAGCCCCAGCCCCAGC------------------------------------------------------------4GENIChomozygous53160201
108507182985071830TC14GENIChomozygous51525093
108507278285072783CT14GENIChomozygous53160203
108507314985073154AAACA-----14GENIChomozygous51525095
108507328685073288GA--19GENIChomozygous53160205
108507402885074029AT20GENIChomozygous51525099
108507589485075895TTG23GENIChomozygous51525100
108507758885077598CACACACACA----------7GENICheterozygous52683309
108507796885077969GA27GENIChomozygous53160207
108507103085071031TTTGGGGATTTAGCTCAGTGGTAGAGCGCTTG4GENIChomozygous52444462
108507758785077588GGCA7GENICheterozygous52444464
108507589585075896TA24GENIChomozygous52570947