chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2105149213105149214CT13GENIChomozygous58998191
2105149292105149293TC9GENIChomozygous58998192
2105150278105150279AG20GENIChomozygous58998193
2105150586105150587CCAT16GENIChomozygous58998194
2105153327105153328CT18GENIChomozygous58998195
2105154796105154797AG15GENIChomozygous58998196
2105158059105158060AC14GENIChomozygous58998197
2105167960105167964CACA----11GENIChomozygous58998200
2105168127105168128TA15GENIChomozygous58998201
2105168149105168150CA17GENIChomozygous58998202
2105169478105169479TG20GENIChomozygous58998203
2105172018105172019AATGTGTG11GENIChomozygous58998204
2105173106105173107CG12GENIChomozygous58998206
2105173736105173737AG15GENIChomozygous58998207
2105177193105177194GC15GENIChomozygous58998208
2105184160105184161CG17GENIChomozygous58998211
2105184939105184941TG--8GENIChomozygous58998215
2105185981105185982CT22GENIChomozygous58998218
2105187467105187468GA19GENIChomozygous58998220
2105188297105188298TC17GENIChomozygous58998221
2105188471105188472GC17GENIChomozygous58998222
2105192349105192350CG17GENICpossibly homozygous58998223
2105192879105192880GT8GENIChomozygous58998224
2105193602105193610AAACAAAC--------8GENIChomozygous58998225
2105194770105194771TTTTTCATG14GENIChomozygous58998227
2105205184105205185GA20GENIChomozygous58998228
2105206338105206339AAT21GENICpossibly homozygous58998230
2105186701105186702TTTC9GENICheterozygous62458442
2105212197105212198TC8GENIChomozygous58998237
2105212245105212246GA11GENIChomozygous58998238
2105212392105212393GA9GENIChomozygous58998239
2105212419105212420AG10GENIChomozygous58998240
2105213822105213823AAT14GENIChomozygous58998241
2105214170105214171TC19GENIChomozygous58998242
2105214871105214872CT11GENIChomozygous58998244
2105215144105215159AAACTATTTTCTAGT---------------8GENIChomozygous58998245
2105215872105215873CG13GENIChomozygous58998246
2105217105105217106AG13GENIChomozygous58998247
2105222413105222414AC27GENIChomozygous58998250