chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117628346117628347TC31GENIChomozygous116672088
8117629628117629629GC59GENIChomozygous116672090
8117633092117633093AG38GENIChomozygous116672092
8117634319117634320GT47GENICheterozygous116672094
8117635049117635050GA54GENICheterozygous116672096
8117636502117636503TC31GENIChomozygous116672098
8117638887117638888CT30GENIChomozygous116672100
8117639104117639105TC36GENIChomozygous116672102
8117639162117639163TC29GENIChomozygous116672104
8117639698117639699CT29GENIChomozygous116672106
8117640268117640269AG46GENIChomozygous116672108
8117640894117640895GA30GENIChomozygous116672110
8117640915117640916CT29GENIChomozygous116672112
8117640953117640954TC32GENIChomozygous116672114
8117641100117641101AG39GENIChomozygous116672116
8117642869117642870GA27GENIChomozygous116672118
8117643636117643637CT33GENIChomozygous116672120
8117644064117644065GA28GENIChomozygous116672122
8117644937117644938GA34GENIChomozygous116672124
8117645043117645044CA41GENIChomozygous116672126
8117645653117645654TC20GENICheterozygous117005931
8117645715117645716TC28GENICheterozygous116988181
8117645950117645951GT22GENIChomozygous116672130
8117646161117646162GC45GENIChomozygous116672132