chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1225874485225874486GC19GENIChomozygous74733186
1225874599225874600TC40GENIChomozygous74733188
1225875162225875163TG68GENICpossibly homozygous74733190
1225875603225875604AG54GENIChomozygous74733192
1225875699225875700CG40GENIChomozygous74733194
1225876515225876516CA33GENICheterozygous74733196
1225876564225876565AT29GENIChomozygous74733198
1225876566225876567AC29GENIChomozygous74733200
1225876792225876793AT30GENIChomozygous74733202
1225876957225876958GA48GENIChomozygous74733204
1225877268225877269CT38GENIChomozygous74733206
1225877359225877360TC51GENIChomozygous74733208
1225877567225877568GA51GENIChomozygous74733210
1225878705225878706CA27GENIChomozygous74733212
1225879382225879383AG60GENIChomozygous74733214
1225879502225879503CT45GENICpossibly homozygous74733216
1225879941225879942GA34GENIChomozygous74733218
1225890808225890809GT62GENIChomozygous74733220
1225900221225900222AG38GENICheterozygous75344706
1225900249225900250AG43GENICheterozygous74733224
1225916086225916087TA31GENIChomozygous74733226
1225916682225916683AG32GENIChomozygous74733228
1225917451225917452CG34GENIChomozygous74733230
1225917505225917506TG24GENIChomozygous74733232
1225917511225917512AC24GENIChomozygous74733234
1225917944225917945GA34GENIChomozygous74733236
1225918023225918024GA45GENIChomozygous74733238
1225918183225918184CT35GENIChomozygous74733240
1225918322225918323GA43GENIChomozygous74733242
1225918913225918914CT8GENICheterozygous74733244
1225918917225918918AT8GENICheterozygous74733246
1225919588225919589GA57GENIChomozygous74733248
1225919630225919631AG51GENIChomozygous74733250
1225921697225921698AG29GENIChomozygous74733252