chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
147868200178682002TC17GENIChomozygous113498091
147868397278683973GA23GENIChomozygous113498092
147868443378684434AG26GENIChomozygous113498093
147868484178684842TG31GENIChomozygous113498094
147868500778685008GT27GENIChomozygous113498095
147868513878685139GT26GENIChomozygous113498096
147868517578685176CG27GENIChomozygous113602587
147868575278685753AG13GENIChomozygous113498097
147868615978686160GA24GENIChomozygous113498098
147868716978687170AG34GENIChomozygous113498099
147868955178689552GT27GENIChomozygous113498100
147868958678689587TG31GENIChomozygous113498101
147869180878691809TC27GENIChomozygous113498102
147869263078692631AG11GENIChomozygous113498103
147869268778692688GT4GENIChomozygous113498104
147869268878692689AG4GENIChomozygous113498105
147869269578692696AT3GENIChomozygous113498106
147869524878695249TC40GENIChomozygous113498108
147869528678695287GA36GENIChomozygous113498109
147869640978696410GA18GENIChomozygous113498110
147869705678697057CT16GENIChomozygous113498111
147869735378697354AG21GENIChomozygous113498112
147870031378700314TC21GENIChomozygous113498114
147870098078700981GT28GENICpossibly homozygous113498115
147870161178701612CT23GENIChomozygous113498116
147870209278702093CT26GENIChomozygous113498117
147870228878702289AC20GENIChomozygous113498118
147870231878702319CT23GENIChomozygous113498119
147870272078702721GA17GENIChomozygous113498120
147870274678702747GA15GENIChomozygous113498121
147870291878702919CT19GENIChomozygous113498122