chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3154514251154514255CGGC----17GENIChomozygous692163214
3154514259154514260CT20GENIChomozygous526947672
3154514276154514277TG22GENIChomozygous524596844
3154514414154514415AAGTCT23GENIChomozygous692163215
3154515300154515301GA19GENIChomozygous524596845
3154515475154515476GA20GENIChomozygous524596846
3154515627154515628GA36GENIChomozygous524596847
3154515681154515682TA26GENIChomozygous524596848
3154515884154515885AG14GENIChomozygous524596849
3154516260154516261TC42GENIChomozygous524596850
3154516490154516491AT25GENIChomozygous524596851
3154516884154516885AG49GENIChomozygous524596852
3154516887154516888GA49GENICpossibly homozygous524596853
3154517156154517157AG28GENIChomozygous524596854
3154517166154517167TG28GENIChomozygous524596855
3154517351154517352G-41GENIChomozygous692163216
3154517632154517633G-25GENIChomozygous692163217
3154517898154517899TC20GENIChomozygous524596856
3154518068154518069GA37GENIChomozygous524596857
3154518158154518159TTA40GENIChomozygous692163218
3154519184154519185CCA8GENICheterozygous692163219
3154519184154519185CCCA8GENICheterozygous692163220
3154519630154519636TCCCTC------17GENIChomozygous692163221
3154519645154519646CG24GENICheterozygous524596858
3154519651154519652GC22GENICheterozygous524596859
3154519872154519873AC28GENIChomozygous524596860
3154519897154519899TT--23GENIChomozygous692163222
3154519985154519986AG37GENIChomozygous524596861
3154520058154520059TC32GENIChomozygous524596862
3154520079154520080GC34GENIChomozygous524596863
3154521686154521687CT31GENIChomozygous524596864
3154521930154521931AAC20GENICheterozygous692163224
3154522134154522135AG25GENIChomozygous524596865