chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
730986873098688CT37GENIChomozygous634589428
730990873099088TC40GENIChomozygous634589429
730999783099979AG36GENIChomozygous634589430
731001163100117CCTG33GENIChomozygous747526088
731001393100140GGT34GENIChomozygous747526089
731001443100145CCG37GENIChomozygous747526090
731001503100151CCG37GENIChomozygous747526091
731002053100206CCAACA38GENIChomozygous747526092
731009613100962CT31GENIChomozygous634589431
731020103102011CT21GENIChomozygous634589432
731020523102053GGA15GENICheterozygous747526093
731030973103098AT15GENIChomozygous634589433
731048093104810TTG5GENICheterozygous747526096
731051303105131TC4GENIChomozygous634589434