chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116816637168166372GC4GENIChomozygous142299121
116816746468167465CT18GENIChomozygous142299122
116816850868168509AG16GENIChomozygous142299123
116816929168169292TC21GENIChomozygous142299124
116817228368172283CCTTTC29GENIChomozygous142273823
116817298668173001TAAAACAAAACAAAA17GENIChomozygous142273824
116817338468173385CT22GENIChomozygous143507160
116817362768173628CG21GENIChomozygous142299126
116817379468173795TA29GENIChomozygous142299127
116817384268173843GA22GENIChomozygous142299128
116817510668175107T20GENIChomozygous142273825
116817694868176949TA12GENIChomozygous142299129
116817721168177212CT18GENIChomozygous142299130
116817859568178596GA16GENIChomozygous142299131
116817991868179919AG21GENIChomozygous142299132
116818036268180363AG19GENIChomozygous142299133
116818185268181854TG21GENIChomozygous142273826
116818231768182318TA19GENIChomozygous142299134
116818258068182580ATATACTGAGACAAACTGATAAA27GENIChomozygous142273827
116818299868182999TC31GENIChomozygous142299135
116818501468185015TC17GENIChomozygous142299137
116818070668180707TG16GENICheterozygous144097819
116818007568180076T22GENIChomozygous144092029
116818007668180077AC22GENIChomozygous144097818