chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2207455195207455196GC15GENICpossibly homozygous60158568
2207457252207457253C-1GENIChomozygous59771431
2207459006207459007AT15GENIChomozygous60158570
2207459233207459234CT1GENIChomozygous59355610
2207461661207461662CT2GENIChomozygous59355611
2207462600207462601CT20GENIChomozygous60158571
2207465862207465863CA17GENIChomozygous59355622
2207466019207466020CA19GENICpossibly homozygous59355623
2207467620207467621AG6GENIChomozygous59355626
2207468323207468324AC25GENICpossibly homozygous59355629
2207469545207469546AAT1GENIChomozygous60158574
2207469813207469814TA2GENIChomozygous59355633
2207475705207475706AG10GENICpossibly homozygous59355636
2207477365207477366GC19GENIChomozygous60158575
2207479965207479966GC17GENICpossibly homozygous60158576
2207480107207480108GGA1GENIChomozygous59355640
2207481089207481090GA7GENIChomozygous59355642