chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121468342514683426TTAAAC9GENIChomozygous50068616
121468365814683659TC26GENIChomozygous50068620
121468512414685125GA24GENIChomozygous50068622
121468679614686797AATTT3GENICheterozygous50068624
121468679614686797AATTTT3GENICheterozygous50560522
121469046314690464TA24GENIChomozygous50068628
121469317314693174AAGT9GENIChomozygous50068646
121469329314693294AT14GENIChomozygous50533176
121469322414693226GA--16GENIChomozygous50533170
121469328614693292GAGAGA------8GENICheterozygous50533172
121469328814693292GAGA----8GENICheterozygous50533174
121469329514693296AT16GENIChomozygous50533178
121469708314697084TC28GENIChomozygous50068656
121470028514700286TTTGTC32GENIChomozygous50068664
121470049914700500GC20GENIChomozygous50068666
121470063614700637CCTTTTTTTTTTTTT6GENICheterozygous50533180
121470063714700639TT--6GENICheterozygous50068668
121470122514701226GC26GENIChomozygous50068672
121470244514702465GTGCTGTGCTGTGCTGTGCT--------------------3GENIChomozygous50533182
121470413214704133TTA21GENIChomozygous50068674
121470415014704151GT25GENIChomozygous50068676
121470415314704154CT27GENIChomozygous50068678
121470492714704928AAACACACAC8GENICheterozygous50560524
121470492714704928AAACACACACAC8GENICpossibly homozygous50533184
121469703914697040CCAAGTTCTGATTTCTGTAAAACTAAGAAGGATGTTCTCCTGCAGCAGG46GENIChomozygous50503954