chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
36219072662190727TC24GENIChomozygous111589060
36219210662192107CT29GENIChomozygous111589061
36219268962192690GA25GENIChomozygous111589062
36219269062192691TC25GENIChomozygous111589063
36219311062193111AG44GENIChomozygous111589064
36219318662193187TG45GENIChomozygous111589065
36219333362193334CA43GENIChomozygous111589066
36219354262193543AT16GENIChomozygous111589067
36219365762193658TC22GENIChomozygous111589068
36219398162193982CT43GENIChomozygous111589069
36219404862194049GA41GENIChomozygous111589070
36219425662194257GT41GENIChomozygous111589071
36219425962194260CT41GENIChomozygous119649649
36219426962194270CA38GENIChomozygous111589072
36219427262194273AT36GENIChomozygous111589073
36219486962194870CT27GENIChomozygous111589074
36219655362196554AC28GENIChomozygous111589082
36219721262197213AC16GENIChomozygous111589085
36219842562198426AG38GENIChomozygous111589088
36219907762199078AC40GENIChomozygous111589089
36219913862199139TC35GENIChomozygous111589090
36219926762199268GT43GENIChomozygous111589091
36219933162199332TC39GENIChomozygous111589092
36219988762199888GA45GENIChomozygous111589093
36219996962199970CT41GENIChomozygous111589094