chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103911024139110242AG51GENIChomozygous116566233
103911037539110376TC28GENIChomozygous116566235
103911061139110612CA65GENIChomozygous116566237
103911086239110863TC41GENIChomozygous117004617
103911150339111504GC42GENIChomozygous117004619
103911197039111971TC41GENIChomozygous116566239
103911250239112503CT36GENIChomozygous117004621
103911273939112740GA60GENIChomozygous116566241
103911457739114578TC33GENIChomozygous117004623
103911507939115080AG75GENIChomozygous116566249
103911512839115129GA79GENIChomozygous117004625
103911635339116354TG30GENIChomozygous116566251
103911645539116456CT39GENIChomozygous117004627