chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151525906151525907GT38GENIChomozygous583714014
5151526027151526028CT20GENIChomozygous583714015
5151526059151526060CT19GENIChomozygous583714016
5151526224151526225AG32GENIChomozygous583714017
5151526430151526432CA--36GENIChomozygous719606214
5151526587151526588CA49GENIChomozygous583714018
5151526927151526928GC44GENIChomozygous583714019
5151527070151527071CT43GENIChomozygous583714020
5151527248151527249GA41GENIChomozygous583714021
5151527609151527610CCTTTTTTTTTT5GENIChomozygous719606216
5151527627151527628T-1GENIChomozygous719606217
5151527704151527705A-13GENIChomozygous719606218
5151527791151527792CT29GENIChomozygous583714022
5151527996151527997GA25GENIChomozygous583714023
5151528016151528017CCTT20GENIChomozygous719606219
5151528037151528038CCTTTTT15GENICheterozygous719606222
5151528037151528038CCTTTTTTTTTT15GENICheterozygous719606223
5151528329151528330GA37GENIChomozygous583714024
5151529316151529332TCAATCAATCAACCAA----------------22GENIChomozygous719606224
5151530452151530453TC58GENIChomozygous583714025
5151531032151531033GA36GENIChomozygous583714026
5151531071151531072TTA38GENICheterozygous719606225
5151531071151531072TTAA38GENICpossibly homozygous719606226
5151532097151532098AAT25GENIChomozygous719606227
5151532349151532350GA23GENIChomozygous583714027
5151532466151532467AT30GENIChomozygous583714028