chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
204427503444275035AG18GENIChomozygous130115759
204429936244299363GT21GENICpossibly homozygous147217020
204429949244299493CT7GENIChomozygous403755261
204429949244299493C7GENICheterozygous403755262
204429950144299502AT6GENIChomozygous403755263
204429950144299502A6GENICheterozygous403755264
204429962744299628CA5GENIChomozygous147217021
204431053244310533A12GENICheterozygous130000784
204431053244310533AC12GENIChomozygous155165551
204431345844313459CT22GENIChomozygous147217022
204432357744323577T15GENICheterozygous130000794