chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
94665953146659532GA26GENIChomozygous117539361
94665953246659533TG26GENIChomozygous117539363
94665955046659550A25GENIChomozygous128708313
94665957046659570A25GENIChomozygous128708314
94665957746659578A25GENIChomozygous128708315
94665963046659631T19GENIChomozygous128708316
94665963946659639T21GENIChomozygous128708317
94665969646659697G21GENIChomozygous128708318
94665972946659730GC22GENIChomozygous117539365
94665973246659733A22GENIChomozygous128708319
94665975246659752T22GENIChomozygous128708320
94665987146659871G8GENIChomozygous128708325
94665978146659781T20GENIChomozygous128708321
94665980746659808A17GENIChomozygous128708322
94665985646659856C8GENIChomozygous128708323
94665986546659865T8GENIChomozygous128708324
94665989246659893G8GENIChomozygous128708326
94665991546659915G7GENIChomozygous128708327
94665991946659920AC6GENIChomozygous117539367
94666137546661376TC16GENIChomozygous117539369
94666373646663737A15GENIChomozygous131066817
94672035946720359AGTAAAGTCAAAACTGGATGGTGAGCTTAAAGCCCCCGTCAATCAACCATTG18GENIChomozygous128708331
94672842046728484TGAACTTTGTCCTACCTTGTTTTTTTTTTTTAAACATTTTTTTTAATCTTTTTATTTTATTTTA5GENIChomozygous128708332
94672874946728750GT20GENICpossibly homozygous117539373
94672876846728769AT22GENIChomozygous117333954
94672877246728772T23GENIChomozygous128708333
94674450746744508GC47GENICheterozygous117333955
94668969046689692AC23GENICheterozygous129958807
94672877546728776AG23GENIChomozygous117706903
94672877646728777GC23GENIChomozygous117706905
94676155646761556TGTA12GENICheterozygous134372835
94676155346761554CT12GENICheterozygous134373482