chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3161038121161038122AG60GENICheterozygous111795832
3161038217161038218CT51GENICheterozygous111795834
3161038252161038253CT43GENICheterozygous112045526
3161038448161038449CT48GENICheterozygous111795836
3161038462161038463CT46GENICheterozygous111795838
3161038480161038481CT58GENICheterozygous111795840
3161038502161038503CT83GENICheterozygous111795842
3161038596161038597AC144GENICheterozygous111795844
3161038607161038608CT157GENICheterozygous112192432
3161038609161038610GA160GENICheterozygous111795846
3161038612161038613AT135GENICheterozygous112045527
3161038634161038635TA233GENICheterozygous111795848
3161038640161038641AC243GENICheterozygous111795850
3161038673161038674CT227GENICheterozygous112045528
3161038678161038679CT209GENICheterozygous112045529
3161038700161038701CT168GENICheterozygous111795852
3161038705161038706CA169GENICheterozygous112396793
3161039250161039251GA34GENIChomozygous111795854
3161039712161039713AG33GENICpossibly homozygous111795856
3161039818161039819GA39GENICheterozygous111795860
3161039995161039996CA79GENICheterozygous111795862
3161040139161040140CT20GENICheterozygous111795864