chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5111817554111817555TC29GENIChomozygous55640419
5111818340111818341AG24GENIChomozygous55640420
5111819025111819026C-6GENIChomozygous55640421
5111819498111819499GC20GENICpossibly homozygous55640422
5111820965111820966GGT1GENIChomozygous56051952
5111821143111821144AG1GENIChomozygous55640425
5111822589111822590CT22GENIChomozygous55640426
5111822983111822985TT--2GENICheterozygous55640427
5111823631111823632T-2GENIChomozygous56051961
5111823727111823728TC9GENIChomozygous55640428
5111824018111824019GGT8GENICpossibly homozygous55640429
5111824295111824296TG5GENIChomozygous55640432
5111824411111824412TTTGTG5GENIChomozygous55640433