chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7119749265119749266TC11GENIChomozygous54082209
7119749355119749356CT20GENIChomozygous54082210
7119749820119749821GT13GENIChomozygous54082211
7119749945119749946AG8GENIChomozygous54082212
7119750047119750048TC21GENIChomozygous54082213
7119750052119750053TC16GENIChomozygous54082214
7119750379119750380TC16GENIChomozygous54082215
7119750601119750602GC12GENIChomozygous54082216
7119750769119750770CT13GENIChomozygous54082217
7119752252119752253GA12GENIChomozygous54082218
7119753842119753843GT10GENIChomozygous54082219
7119753882119753883CT15GENIChomozygous54082220
7119754586119754594GCACTCAC--------7GENICheterozygous55095808
7119755109119755110GA14GENIChomozygous54082222
7119755507119755508AG12GENIChomozygous54082223
7119755859119755860TC11GENIChomozygous54082224
7119756034119756035CT6GENIChomozygous54082225
7119756038119756039CT6GENIChomozygous54082226
7119756112119756113GA6GENIChomozygous54082227
7119756187119756188A-7GENIChomozygous54082228
7119756220119756221GA10GENIChomozygous54082229
7119754587119754597CACTCACGCA----------7GENICheterozygous55631723