chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151526027151526028CT29GENICpossibly homozygous580279486
5151526059151526060CT30GENICpossibly homozygous580279487
5151526224151526225AG11GENIChomozygous580279488
5151526430151526432CA--4GENICheterozygous717656005
5151526587151526588CA12GENICpossibly homozygous580279489
5151526927151526928GC25GENIChomozygous580279490
5151527070151527071CT20GENICpossibly homozygous580279491
5151527248151527249GA26GENICpossibly homozygous580279492
5151527791151527792CT9GENICpossibly homozygous580279493
5151527996151527997GA9GENICpossibly homozygous580279494
5151528016151528017CCTT1GENIChomozygous717656006
5151528329151528330GA3GENIChomozygous580279495
5151530452151530453TC24GENICpossibly homozygous580279496
5151531032151531033GA18GENICpossibly homozygous580279497
5151531071151531072TTAA2GENIChomozygous717656008
5151532097151532098AAT4GENIChomozygous717656009
5151532349151532350GA14GENIChomozygous580279498
5151532466151532467AT16GENIChomozygous580279499