chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174544000345440004AG51GENIChomozygous809763641
174544022445440225TG38GENICheterozygous809763642
174544060645440607AG48GENICpossibly homozygous809763643
174544116745441168TC58GENIChomozygous809763644
174544333945443340TC41GENIChomozygous809763645
174544360345443604TA12GENICheterozygous809763646
174544363945443640GA21GENIChomozygous809763647
174544370845443709TC34GENIChomozygous809763648
174544484745444848AT55GENICpossibly homozygous809763649
174544625645446257TC26GENIChomozygous809763650
174544660945446610AG24GENIChomozygous809763651