chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2189858716189858717AG11GENIChomozygous110172125
2189859499189859500TC24GENIChomozygous110172127
2189860331189860332AG24GENIChomozygous110805135
2189860932189860933TA12GENICpossibly homozygous110172130
2189861052189861053A23GENICheterozygous129869183
2189861071189861071A28GENIChomozygous127718060
2189863286189863287AC17GENIChomozygous110172132
2189864653189864654AG24GENIChomozygous110172136
2189868876189868881TATAT11GENIChomozygous132017873
2189868889189868890CT22GENIChomozygous110172144
2189869050189869051GC2GENIChomozygous132033653
2189869859189869860GT26GENIChomozygous110172146
2189870557189870558TC8GENIChomozygous120351053
2189870783189870784T6GENIChomozygous132017874
2189872714189872715A23GENIChomozygous132017875
2189874150189874151CG21GENIChomozygous110172148
2189874299189874299CCCTGG20GENICheterozygous132017876
2189874304189874304TAGCAATGAATATCCTAGTAAGAGC20GENICheterozygous132566993
2189874306189874307AC17GENICheterozygous132578146
2189875021189875022TC22GENIChomozygous110172150
2189874287189874287AAAAAAAATAAAAAAAAAAAA10GENICheterozygous134514458