chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5141057947141057948CCG34GENIChomozygous56235386
5141058339141058340CCAG49GENIChomozygous55753822
5141058762141058763GGA14GENICpossibly homozygous55753823
5141058762141058763GGAA14GENICheterozygous56457912
5141060465141060466GGAAA15GENICheterozygous55907576
5141060465141060466GGA15GENICheterozygous55907578
5141060893141060894GA40GENIChomozygous56235387
5141062649141062650TTGG40GENIChomozygous55753827
5141063075141063076GA19GENIChomozygous56235388
5141063576141063577CT21GENIChomozygous56188107
5141063618141063620AA--6GENICheterozygous55753829
5141063619141063620A-6GENICheterozygous56457913
5141064783141064784TTTGGTGG6GENIChomozygous56493993
5141066526141066527CT37GENIChomozygous56235389
5141067398141067399GT36GENIChomozygous56235391
5141068528141068529TTAATAAATA4GENIChomozygous56493994