chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101403357914033583TTTT----22GENICpossibly homozygous759277207
101403406114034062TC13GENIChomozygous653713006
101403420714034208AAAT7GENIChomozygous759277209
101403433814034339A-12GENIChomozygous759277210
101403462714034628GA22GENIChomozygous653713007
101403486914034870CA26GENIChomozygous653713008
101403531514035316CCAAAA4GENICheterozygous759277213
101403531614035319AAA---4GENICheterozygous759277211
101403531714035319AA--4GENICheterozygous759277212
101403675914036760A-20GENIChomozygous759277214
101403733314037334GC15GENIChomozygous653713009
101403920514039206TC30GENIChomozygous653713010
101404104614041054GTGTGTGT--------16GENICheterozygous759277215
101404104814041054GTGTGT------16GENICpossibly homozygous759277216
101404111414041115AATGTGTGTGTAGTATGTGG9GENIChomozygous759277219
101404375314043754AG33GENIChomozygous653713011
101404423614044237TC39GENIChomozygous653713012
101404493714044941TTTG----16GENIChomozygous759277220
101404532914045330GA28GENIChomozygous653713013
101404540014045401TTTCCTGGGAGC20GENIChomozygous759277222