chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1225874485225874486GC40GENIChomozygous74733186
1225874599225874600TC31GENIChomozygous74733188
1225875162225875163TG19GENICpossibly homozygous74733190
1225875603225875604AG18GENIChomozygous74733192
1225875699225875700CG30GENIChomozygous74733194
1225876564225876565AT23GENIChomozygous74733198
1225876566225876567AC23GENIChomozygous74733200
1225876792225876793AT44GENIChomozygous74733202
1225876957225876958GA28GENIChomozygous74733204
1225877268225877269CT30GENIChomozygous74733206
1225877359225877360TC37GENIChomozygous74733208
1225877567225877568GA27GENIChomozygous74733210
1225878705225878706CA36GENIChomozygous74733212
1225879382225879383AG27GENIChomozygous74733214
1225879502225879503CT36GENIChomozygous74733216
1225879941225879942GA48GENIChomozygous74733218
1225890808225890809GT29GENIChomozygous74733220
1225916086225916087TA34GENIChomozygous74733226
1225916682225916683AG40GENIChomozygous74733228
1225917451225917452CG57GENIChomozygous74733230
1225917505225917506TG38GENIChomozygous74733232
1225917511225917512AC40GENIChomozygous74733234
1225917944225917945GA41GENIChomozygous74733236
1225918023225918024GA41GENIChomozygous74733238
1225918183225918184CT29GENIChomozygous74733240
1225918322225918323GA48GENIChomozygous74733242
1225919588225919589GA51GENIChomozygous74733248
1225919630225919631AG42GENIChomozygous74733250