chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
36163442761634428CT49GENICpossibly homozygous978540334
36163448961634490GA38GENIChomozygous978540335
36163452761634528CT41GENIChomozygous978540336
36163942761639428CT45GENIChomozygous978540337
36164179761641798CT38GENIChomozygous978540338
36164254861642549CT17GENIChomozygous978540339
36164285361642854GA47GENIChomozygous978540340
36164592661645927TG43GENIChomozygous978540341
36164626261646263AT30GENIChomozygous978540342
36164699061646991TA26GENIChomozygous978540343
36164989761649898AG21GENIChomozygous978540344
36165034561650346TG39GENIChomozygous978540345
36165072661650727AG19GENIChomozygous978540346