chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103851292238512923AG42GENIChomozygous116565369
103851303138513032TC29GENIChomozygous117004286
103851328238513283GA26GENIChomozygous117004288
103851472438514725GA22GENIChomozygous116761903
103851492438514925AG33GENIChomozygous116761905
103851528938515290AG28GENIChomozygous116761909
103851537738515378TA28GENIChomozygous117004290
103851606038516061TC31GENIChomozygous116761911
103851661938516620GA32GENIChomozygous117004292
103851854838518549GA19GENIChomozygous117004294
103852047838520479CT31GENIChomozygous116761915
103852304138523042CT37GENIChomozygous117004296
103852392938523930CA35GENIChomozygous117004298
103852430438524305TC43GENIChomozygous116761919
103852486238524863AG25GENIChomozygous116761925
103852584138525842AG39GENIChomozygous116761927
103852609638526097TC29GENIChomozygous117004300
103852750338527504AG19GENIChomozygous116761931
103852864038528641CT30GENIChomozygous117004302
103853223638532237AC21GENIChomozygous117004304
103853376238533763CT31GENIChomozygous117004306