chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3161038448161038449CT25GENICheterozygous111795836
3161038462161038463CT27GENICheterozygous111795838
3161038480161038481CT40GENICheterozygous111795840
3161038502161038503CT52GENICheterozygous111795842
3161038596161038597AC44GENICheterozygous111795844
3161038607161038608CT45GENICheterozygous112192432
3161038609161038610GA44GENICheterozygous111795846
3161038612161038613AT39GENICheterozygous112045527
3161038618161038619CA64GENICheterozygous112192433
3161038634161038635TA105GENICheterozygous111795848
3161038640161038641AC109GENICheterozygous111795850
3161038673161038674CT112GENICheterozygous112045528
3161038678161038679CT107GENICheterozygous112045529
3161038700161038701CT70GENICheterozygous111795852
3161039250161039251GA26GENIChomozygous111795854
3161039712161039713AG42GENICpossibly homozygous111795856
3161039995161039996CA42GENICheterozygous111795862