chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1225874485225874486GC11GENIChomozygous74733186
1225874599225874600TC8GENIChomozygous74733188
1225875162225875163TG11GENIChomozygous74733190
1225875603225875604AG6GENIChomozygous74733192
1225875699225875700CG17GENIChomozygous74733194
1225876564225876565AT10GENIChomozygous74733198
1225876566225876567AC11GENIChomozygous74733200
1225876792225876793AT14GENIChomozygous74733202
1225876957225876958GA21GENIChomozygous74733204
1225877268225877269CT10GENIChomozygous74733206
1225877359225877360TC13GENIChomozygous74733208
1225877567225877568GA25GENICpossibly homozygous74733210
1225878705225878706CA19GENIChomozygous74733212
1225879382225879383AG27GENIChomozygous74733214
1225879502225879503CT14GENIChomozygous74733216
1225879941225879942GA23GENIChomozygous74733218
1225890808225890809GT10GENIChomozygous74733220
1225916086225916087TA17GENIChomozygous74733226
1225916682225916683AG20GENIChomozygous74733228
1225917451225917452CG23GENIChomozygous74733230
1225917505225917506TG30GENIChomozygous74733232
1225917511225917512AC30GENIChomozygous74733234
1225917944225917945GA15GENIChomozygous74733236
1225918023225918024GA20GENIChomozygous74733238
1225918183225918184CT17GENIChomozygous74733240
1225918322225918323GA13GENIChomozygous74733242
1225919588225919589GA9GENIChomozygous74733248
1225919630225919631AG9GENIChomozygous74733250