chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121468342514683426TTAAACAAACAAAC10GENIChomozygous50878722
121468365814683659TC19GENIChomozygous50068620
121468460414684612TGTGTGTG--------4GENICheterozygous50533168
121468512414685125GA15GENIChomozygous50068622
121468679614686797AATTT4GENICheterozygous50068624
121468679614686797AATT4GENICheterozygous50068626
121468679614686797AATTTT4GENICheterozygous50560522
121469046314690464TA28GENIChomozygous50068628
121469317314693174AAGT34GENIChomozygous50068646
121469322414693226GA--25GENIChomozygous50533170
121469328614693292GAGAGA------12GENICheterozygous50533172
121469328814693292GAGA----12GENICheterozygous50533174
121469329314693294AT22GENIChomozygous50533176
121469329514693296AT23GENIChomozygous50533178
121469708314697084TC25GENIChomozygous50068656
121470028514700286TTTGTC19GENIChomozygous50068664
121470049914700500GC14GENIChomozygous50068666
121470063614700637CCTTTTTTTTTTTTT6GENICheterozygous50533180
121470063714700639TT--6GENICheterozygous50068668
121470122514701226GC19GENIChomozygous50068672
121470244514702465GTGCTGTGCTGTGCTGTGCT--------------------5GENIChomozygous50533182
121470413214704133TTA14GENIChomozygous50068674
121470415014704151GT14GENIChomozygous50068676
121470415314704154CT14GENIChomozygous50068678
121470492714704928AAACACACACAC7GENIChomozygous50533184
121469703914697040CCAAGTTCTGATTTCTGTAAAACTAAGAAGGATGTTCTCCTGCAGCAGG29GENIChomozygous50503954