chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4208492832208492833TTA7GENICheterozygous58369111
4208492880208492881AG24GENIChomozygous57066601
4208495077208495078AG15GENIChomozygous57066602
4208497974208497976TT--8GENICheterozygous58369113
4208497975208497976T-8GENICheterozygous58369115
4208498471208498472TC13GENIChomozygous57066605
4208498924208498925TC16GENIChomozygous57066606
4208500571208500572CCTT3GENICheterozygous58369119
4208500597208500602GGTTC-----7GENICheterozygous58447434
4208502120208502121GA34GENIChomozygous57066608
4208504256208504257A-24GENIChomozygous57066609
4208505297208505298TC16GENIChomozygous57066610
4208508035208508036CT21GENIChomozygous57066611
4208510297208510307GAGAGAGAGA----------5GENICheterozygous58369121
4208510543208510544TC21GENIChomozygous57066613
4208512238208512239A-12GENIChomozygous57066614
4208512907208512908TC17GENIChomozygous57066615
4208515943208515944AG33GENIChomozygous57066616
4208521280208521281CT20GENICpossibly homozygous57066617
4208521727208521728CT24GENIChomozygous57066618
4208522139208522142TGG---8GENIChomozygous57066619
4208522353208522354TC14GENIChomozygous57066620
4208523079208523080AG13GENIChomozygous57066621
4208529635208529642TTCGTGG-------17GENIChomozygous57066622
4208533558208533559AG21GENIChomozygous57066628
4208529860208529861GC27GENIChomozygous57066623
4208531069208531070CT26GENIChomozygous57066624
4208531771208531772AT21GENIChomozygous57066625
4208532744208532745CT20GENIChomozygous57066626
4208533095208533096GA21GENIChomozygous57066627
4208530350208530353AAA---12GENIChomozygous57607799