chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3131502722131502723AACTGT52GENIChomozygous57679430
3131503512131503513AAT41GENIChomozygous57679432
3131504806131504807AG51GENIChomozygous57679433
3131509121131509126ACACA-----19GENICheterozygous57679437
3131509123131509126ACA---20GENICheterozygous57679439
3131515043131515044CCT17GENIChomozygous58197670
3131515043131515044CT36GENICheterozygous58478435
3131516187131516188AG15GENIChomozygous57679457
3131516214131516218AAAC----19GENICpossibly homozygous57679460
3131516227131516230AAC---21GENIChomozygous57679464
3131516228131516230AC--24GENIChomozygous57679466
3131516230131516231A-20GENICpossibly homozygous57679468
3131516520131516521AG68GENIChomozygous58197672
3131517604131517605AG61GENIChomozygous58197674
3131518251131518252TTCACA14GENIChomozygous57679480
3131518424131518433CATTGAACT---------25GENIChomozygous58197676
3131519290131519291AAACACAC5GENICheterozygous57679484
3131519290131519291AAACAC5GENICheterozygous58322623