chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X7143590671435907CCAG27GENICheterozygous45260199
X7143600071436001AAAG39GENIChomozygous45260200
X7143629271436294AC--42GENIChomozygous45260201
X7143639271436393GA35GENIChomozygous45260202
X7143651071436511AAG37GENIChomozygous45260203
X7143683971436840TC49GENIChomozygous45146782
X7143685671436857GA56GENIChomozygous45260204
X7143986571439866GA79GENIChomozygous45260205
X7144092171440922GC67GENIChomozygous45260206
X7144183971441840TC51GENIChomozygous45260207
X7144261071442611AG48GENIChomozygous45260208
X7144293571442936CCA55GENIChomozygous45146783
X7144307071443071TC23GENICpossibly homozygous45260209
X7144346071443461TC45GENICpossibly homozygous45260210