chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4144986321144986322GC42GENIChomozygous775093016
4144989080144989081TC32GENIChomozygous775093017
4144989081144989082TA31GENIChomozygous775093018
4144990709144990710TC36GENIChomozygous775093019
4144992768144992769AG25GENIChomozygous775093020
4145001081145001082GA36GENIChomozygous775093021
4145002673145002674GA43GENICpossibly homozygous775093022
4145009034145009035CG43GENIChomozygous775093023