chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4208492832208492833TTA12GENICheterozygous58369111
4208492880208492881AG18GENIChomozygous57066601
4208495077208495078AG34GENIChomozygous57066602
4208497975208497976T-12GENIChomozygous58369115
4208498471208498472TC27GENIChomozygous57066605
4208498924208498925TC37GENIChomozygous57066606
4208499666208499667CCT4GENICheterozygous58369117
4208499667208499668T-4GENICheterozygous57066607
4208500571208500572CCTT5GENICheterozygous58369119
4208500597208500602GGTTC-----14GENICheterozygous58447434
4208502120208502121GA27GENIChomozygous57066608
4208504256208504257A-28GENIChomozygous57066609
4208505297208505298TC43GENICpossibly homozygous57066610
4208508035208508036CT34GENICpossibly homozygous57066611
4208510297208510307GAGAGAGAGA----------1GENIChomozygous58369121
4208510543208510544TC18GENIChomozygous57066613
4208512238208512239A-15GENICpossibly homozygous57066614
4208512907208512908TC33GENIChomozygous57066615
4208515943208515944AG32GENIChomozygous57066616
4208521280208521281CT33GENIChomozygous57066617
4208521727208521728CT20GENIChomozygous57066618
4208522139208522142TGG---8GENIChomozygous57066619
4208522353208522354TC21GENICpossibly homozygous57066620
4208523079208523080AG32GENIChomozygous57066621
4208529635208529642TTCGTGG-------25GENIChomozygous57066622
4208529860208529861GC23GENIChomozygous57066623
4208530350208530353AAA---22GENIChomozygous57607799
4208531069208531070CT29GENIChomozygous57066624
4208531771208531772AT34GENIChomozygous57066625
4208532744208532745CT32GENIChomozygous57066626
4208533095208533096GA27GENICpossibly homozygous57066627
4208533558208533559AG33GENIChomozygous57066628