chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109413702694137027AC54GENIChomozygous116826030
109413745594137456GT47GENIChomozygous116826032
109413812294138123AG61GENIChomozygous116826034
109413864394138644CA56GENICpossibly homozygous116826036
109413869594138696GA61GENIChomozygous116826038
109414016194140162CT36GENIChomozygous116826040
109414075194140752C52GENIChomozygous128847254
109414075794140757C52GENIChomozygous128847255
109414087294140873AG63GENIChomozygous116826042
109414160694141607AG72GENIChomozygous116826044
109414303894143039CA54GENIChomozygous116826046
109414339894143400CC57GENIChomozygous128847256
109414611894146118TGAGCT51GENIChomozygous128847257
109414665994146660GC58GENIChomozygous116826048
109414737994147379C38GENIChomozygous128847258
109414739994147399C40GENIChomozygous128847259
109414740994147409G40GENIChomozygous128847260
109414741894147418G44GENIChomozygous128847261
109414742694147426C41GENIChomozygous128847262
109414744394147443G35GENIChomozygous128847263
109414744894147449C31GENIChomozygous128847264
109414746994147469C29GENIChomozygous128847265
109414749594147495C27GENIChomozygous128847266
109414756194147562TG19GENIChomozygous123407997
109414756294147563GC19GENIChomozygous123407998
109414748594147486CG27GENIChomozygous118076117
109414287394142874TC58GENIChomozygous116684629
109414362794143628AC45GENIChomozygous116684631