chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77355942873559429AG41GENICheterozygous54656906
77356040773560408TA22GENIChomozygous54200966
77356077673560777TTC20GENIChomozygous53969996
77356078173560782GGT21GENIChomozygous53969998
77356398073563981TTACAC9GENICheterozygous53970029
77356407873564079TTACACAC13GENICheterozygous53970033
77356407973564083ACAC----13GENICheterozygous54200972
77356421473564215CT22GENICheterozygous53970035
77356422473564225GA21GENICheterozygous53970037
77356766073567662GC--7GENICheterozygous53970049
77356772973567731CA--5GENICheterozygous53970057
77356773773567739CA--6GENICheterozygous53970059
77356424273564243CT23GENICheterozygous54447804
77356776073567762GT--6GENICheterozygous54447806
77357397773573979AT--20GENICheterozygous53970125
77357678973576790AC10GENIChomozygous53970149
77357681273576813G-7GENIChomozygous53970151
77357794673577947TA21GENICpossibly homozygous53970183
77358306873583069G-8GENIChomozygous53970259
77358307473583075CA8GENIChomozygous53970261
77358359273583593GA43GENIChomozygous53970265
77358391873583919G-21GENIChomozygous53970267
77358443973584440G-18GENIChomozygous53970275
77358531673585317G-27GENIChomozygous53970281