chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1225874485225874486GC46GENIChomozygous74733186
1225874599225874600TC69GENICpossibly homozygous74733188
1225875162225875163TG64GENICpossibly homozygous74733190
1225875603225875604AG82GENIChomozygous74733192
1225875699225875700CG78GENIChomozygous74733194
1225876515225876516CA35GENICheterozygous74733196
1225876564225876565AT28GENIChomozygous74733198
1225876566225876567AC28GENICpossibly homozygous74733200
1225876792225876793AT45GENIChomozygous74733202
1225876957225876958GA73GENIChomozygous74733204
1225877268225877269CT75GENIChomozygous74733206
1225877359225877360TC50GENIChomozygous74733208
1225877567225877568GA57GENIChomozygous74733210
1225878705225878706CA51GENIChomozygous74733212
1225879382225879383AG61GENIChomozygous74733214
1225879502225879503CT47GENIChomozygous74733216
1225879941225879942GA58GENIChomozygous74733218
1225890808225890809GT76GENIChomozygous74733220
1225900217225900218AG47GENICheterozygous75792715
1225900221225900222AG41GENICheterozygous75344706
1225916086225916087TA39GENIChomozygous74733226
1225916682225916683AG68GENIChomozygous74733228
1225917451225917452CG65GENIChomozygous74733230
1225917505225917506TG58GENIChomozygous74733232
1225917511225917512AC57GENIChomozygous74733234
1225917944225917945GA57GENIChomozygous74733236
1225918023225918024GA61GENIChomozygous74733238
1225918183225918184CT53GENIChomozygous74733240
1225918322225918323GA78GENIChomozygous74733242
1225918913225918914CT20GENICheterozygous74733244
1225918917225918918AT14GENICheterozygous74733246
1225919588225919589GA53GENIChomozygous74733248
1225919630225919631AG48GENIChomozygous74733250
1225921697225921698AG50GENIChomozygous74733252
1225918927225918928CT15GENICheterozygous76669032