chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185701606057016061AG11GENIChomozygous63900853
185701722157017222AC23GENIChomozygous63900854
185701727357017274AG23GENIChomozygous63900855
185701985957019860AC16GENIChomozygous63900861
185701877357018774CT17GENICpossibly homozygous64043176
185702121957021220AC28GENIChomozygous64043179
185702597557025976CT27GENICpossibly homozygous63900870
185702597957025980CT28GENICpossibly homozygous63900871
185702613357026134TG27GENIChomozygous64043185
185702630057026301GC22GENIChomozygous63900872
185702701957027020AG15GENIChomozygous63900873
185702715157027152AT22GENIChomozygous64043188
185702970257029703TG24GENIChomozygous64043191
185702992757029928CT32GENIChomozygous64043194
185703235057032351AG20GENIChomozygous63900884
185703288457032885CA25GENICpossibly homozygous63900887
185703288657032887CA24GENICpossibly homozygous63900888
185703641357036414GA22GENIChomozygous63900893
185703702957037030CG24GENIChomozygous64043197
185703772157037722AT37GENIChomozygous63900894
185703811257038113GA23GENIChomozygous64043200
185703832857038329AG16GENIChomozygous63900897
185703954557039546TC28GENIChomozygous63900899
185703965857039659TC30GENICpossibly homozygous63900900
185704111857041119TG19GENIChomozygous64043203
185704243057042431GA21GENIChomozygous63900903
185704274757042748AG29GENIChomozygous63900904
185704281357042814TC28GENIChomozygous63900905
185704417957044180AG17GENIChomozygous63900909
185704588257045883CG17GENICpossibly homozygous64043209
185704611857046119GA17GENIChomozygous64043212
185704710357047104CT28GENIChomozygous64043215
185704820757048208CT22GENIChomozygous64043218
185704880457048805GC12GENIChomozygous64043223
185705063257050633AG33GENIChomozygous63900928
185705079957050800CT31GENIChomozygous64043226
185705285457052855AG26GENIChomozygous64043231
185705290357052904CT23GENIChomozygous64043234
185705349057053491AG27GENIChomozygous64043237