chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
591772609177261GA59GENIChomozygous793778212
591775089177509GC29GENIChomozygous793778213
591775219177522TC29GENIChomozygous793778214
591777129177713TC43GENIChomozygous793778215
591778639177864AG29GENIChomozygous793778216
591782059178206TC46GENIChomozygous793778217
591782109178211TC44GENIChomozygous793778218
591784379178438GT29GENICheterozygous793778219
591784409178441CT32GENICheterozygous793778220
591792239179224GA42GENIChomozygous793778221
591792919179292TC33GENIChomozygous793778222
591795329179533GA27GENICpossibly homozygous793778223
591797569179757GT26GENIChomozygous793778224
591798379179838CA22GENIChomozygous793778225
591800589180059CT27GENICpossibly homozygous793778226
591800649180065GA29GENICpossibly homozygous793778227
591805859180586CT27GENIChomozygous793778228