chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15151761551517616CT22GENIChomozygous109279215
15151807051518071TC32GENIChomozygous109279217
15151829951518300TG28GENICpossibly homozygous109279219
15151849151518492TG28GENIChomozygous109279221
15151857951518580CG34GENIChomozygous109279223
15151929351519294TC21GENIChomozygous109279225
15152052951520530GC40GENIChomozygous109279228
15152054051520541AG40GENIChomozygous108847664
15152058251520583TC30GENIChomozygous109279230
15152163651521637CA12GENIChomozygous108095750
15152188051521881CA19GENIChomozygous109279232
15152344151523442GC27GENIChomozygous108847667
15152345551523456TC28GENIChomozygous108847668
15152603351526034TC26GENIChomozygous108847672