chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91409145814091459CG33GENICpossibly homozygous52601623
91409235414092364ACACACACAC----------7GENICpossibly homozygous51761562
91409248614092487TTG23GENIChomozygous51761564
91409259214092593A-34GENIChomozygous51761568
91409265814092662CACA----15GENICheterozygous51761570
91409266014092662CA--15GENICheterozygous52601626
91409389214093893CG43GENIChomozygous51761574
91409698614096987T-3GENIChomozygous51761576
91409700814097009GGAA2GENICheterozygous52173720
91409706514097066TTGCG10GENIChomozygous51761578
91409730214097303CT22GENIChomozygous52601629
91410066714100668GT33GENIChomozygous51761585
91410108614101087C-20GENIChomozygous52601632
91410116614101182ACACACACACACACAC----------------5GENICheterozygous52173722
91410479414104795TC10GENIChomozygous51761589
91410570314105704TC40GENIChomozygous51761593
91410631314106314TC39GENIChomozygous51761597
91410698614106987TTC25GENICheterozygous52527036
91410718114107182GGGA29GENIChomozygous51761601
91410718414107185GGAT22GENIChomozygous51761603
91410725514107257AT--29GENIChomozygous52601636