chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2207867832207867833CCCACA14GENICheterozygous60561311
2207867832207867833CCCACACA14GENICheterozygous60561312
2207868353207868354A-32GENICpossibly homozygous59356619
2207869356207869357CT23GENIChomozygous59356623
2207869592207869593CT34GENIChomozygous59356624
2207871200207871201AG10GENIChomozygous59356626
2207871595207871596GGCCTGGCT19GENIChomozygous59356627
2207872469207872470GGTTTGTTT16GENIChomozygous59356630
2207873593207873594TTTC8GENICpossibly homozygous59356631