chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170597092170597093CT27GENIChomozygous120678556
1170601709170601710AT32GENIChomozygous108376219
1170606060170606061GA26GENIChomozygous120678558
1170606236170606237AG19GENIChomozygous108376223
1170608629170608630CT23GENIChomozygous120678560
1170609804170609805TC20GENIChomozygous120678562
1170609945170609946TC23GENIChomozygous108376236
1170610794170610795AG16GENIChomozygous108376238
1170612829170612830GA19GENIChomozygous120678564
1170615839170615840CT19GENIChomozygous108376248
1170618203170618204GT22GENIChomozygous120678566
1170619031170619032CT20GENIChomozygous108376254
1170619874170619875TA20GENICpossibly homozygous120678568
1170620820170620821TG24GENIChomozygous108376258
1170615184170615185C16GENIChomozygous127455559
1170615343170615344G17GENIChomozygous127455560
1170622757170622758TC21GENIChomozygous108376262
1170623786170623787CT12GENIChomozygous120678570
1170623879170623880CT15GENIChomozygous120678572
1170627644170627645GA24GENIChomozygous120678574