chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1186054267186054268AG27GENIChomozygous108450385
1186054314186054315GA35GENIChomozygous108450387
1186054447186054448AC30GENIChomozygous108450389
1186059435186059436TC34GENIChomozygous108450391
1186059448186059449AG36GENIChomozygous108450393
1186062124186062125GT40GENIChomozygous108450397
1186062713186062714TC30GENIChomozygous108450399
1186063817186063818GA17GENIChomozygous108450401
1186063949186063950AC26GENIChomozygous108450403
1186063990186063991GA22GENIChomozygous108450405
1186064525186064526TC38GENIChomozygous108450407
1186064526186064527GA38GENIChomozygous108450409
1186064756186064757TA22GENIChomozygous108450411
1186065086186065087CT27GENIChomozygous108450413
1186065874186065875CT35GENIChomozygous108450415
1186066290186066291TG47GENIChomozygous108450417