chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113037401230374013AT7GENIChomozygous115959551
113037429630374297CT43GENIChomozygous115808379
113037533030375331TC29GENIChomozygous115808381
113038458430384585AC26GENIChomozygous115808383
113038493030384931GA31GENIChomozygous115808385
113038573530385736TA45GENIChomozygous115808387
113038600330386004AG32GENIChomozygous115808389
113038712430387125CT43GENIChomozygous115808391
113038995330389954CT43GENIChomozygous116351237
113039010930390110AG36GENIChomozygous116351238
113039099230390993GT22GENIChomozygous115808395
113039191030391911GC35GENIChomozygous115959559
113039357630393577GC43GENIChomozygous115808397
113039436530394366GA33GENIChomozygous116351239
113039486530394866GA35GENIChomozygous115808399
113039509030395091TC8GENIChomozygous116351240
113039727430397275CT16GENIChomozygous115808401
113039900330399004CA20GENIChomozygous116351241
113040284630402847CT53GENIChomozygous115808403
113040320430403205CT19GENIChomozygous116351242
113040843730408438CT24GENIChomozygous116351243
113041015530410156CG12GENIChomozygous116266777
113041271130412712AG30GENIChomozygous115808405
113041306930413070AG19GENIChomozygous115808407
113041320530413206AC22GENIChomozygous115808409
113041446230414463TC34GENIChomozygous116351244
113041478730414788CT25GENIChomozygous115808411
113041528730415288TG39GENIChomozygous115808415
113041550030415501AG55GENIChomozygous115808417
113041551330415514GA43GENICpossibly homozygous116109572
113041839730418398TA7GENIChomozygous116351245
113042346330423464AG17GENICpossibly homozygous115808421
113042395730423958GT37GENIChomozygous115808423
113042574930425750TC14GENIChomozygous116351247
113042633430426335TC31GENIChomozygous115959573
113042645730426458TA13GENIChomozygous115808425