chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117052277117052278AT24GENIChomozygous579839245
8117052890117052891AG21GENICpossibly homozygous579839246
8117053035117053036AG18GENICpossibly homozygous579839247
8117054122117054123CT18GENICpossibly homozygous579839248
8117054158117054159AG4GENICheterozygous579839249
8117055369117055370TC25GENIChomozygous579839250
8117056118117056119GGA24GENIChomozygous717813197
8117056327117056328CA24GENIChomozygous579839251
8117056459117056460GA23GENICpossibly homozygous581372732
8117057218117057219T-24GENIChomozygous717813198
8117058388117058389AG13GENICpossibly homozygous579839252
8117059204117059205AC20GENIChomozygous579839253
8117060015117060016GA24GENICpossibly homozygous581372733
8117060807117060808CT18GENIChomozygous579839254
8117061256117061257CT20GENIChomozygous581372734
8117061986117061987CT18GENIChomozygous579839255
8117062214117062215CT11GENIChomozygous579839256
8117062340117062341TTGTCA4GENIChomozygous717813199
8117062839117062840CG14GENICpossibly homozygous579839257
8117063514117063515CT8GENIChomozygous579839258
8117063641117063642GC8GENICheterozygous579839259
8117063787117063788TC20GENICpossibly homozygous579839260
8117067190117067191GGCTGT8GENIChomozygous717813200
8117067250117067251AG7GENIChomozygous579839261
8117067587117067588TC8GENICheterozygous579839262
8117068510117068511AG20GENIChomozygous579839263
8117068570117068571TC25GENICpossibly homozygous579839264
8117068680117068681CA12GENIChomozygous579839265
8117068800117068801AG13GENIChomozygous579839266
8117068936117068937TTTC15GENICpossibly homozygous717813201
8117069221117069222GA1GENIChomozygous579839267
8117070028117070029TC18GENIChomozygous579839268
8117070774117070775TA4GENICheterozygous581372735
8117072502117072503TC12GENIChomozygous579839269
8117072674117072675AATG6GENICheterozygous717813202
8117074996117074997AG16GENIChomozygous579839270