chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117026371117026371TCAGTGTTTC50GENICheterozygous131874545
7117027006117027007TC57GENICheterozygous116301941
7117027421117027422GA37GENICheterozygous116301942
7117027840117027840T40GENICheterozygous131874546
7117028986117028987GA43GENIChomozygous116301943
7117029038117029039TC40GENIChomozygous116301944
7117029079117029080GA40GENIChomozygous116301945
7117029533117029534AC51GENICheterozygous116301946
7117030099117030100CT62GENICheterozygous116301947
7117030285117030286GA48GENIChomozygous116301948
7117030621117030622GA41GENIChomozygous116301949
7117030794117030795GA98GENICheterozygous116301950
7117031833117031834AG54GENIChomozygous115846119
7117027441117027441TTATCTTTTTGGTCAGGAGA30GENICheterozygous131023948
7117030243117030244A66GENICheterozygous131023949
7117027912117027913GA32GENICheterozygous131040236
7117027915117027916CG32GENICheterozygous131040237
7117030511117030512GA49GENICheterozygous131040238
7117027919117027920GA32GENIChomozygous116393555
7117028010117028011CT34GENICheterozygous131882362
7117031156117031157CT61GENICheterozygous131882363
7117031188117031189GA72GENICheterozygous131882364
7117032498117032500CT44GENICheterozygous128510424
7117032582117032583AG29GENIChomozygous115846123
7117032865117032866TC36GENICheterozygous128562329