chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121468365814683659TC17GENICpossibly homozygous597136492
121468512414685125GA15GENIChomozygous597136493
121469046314690464TA29GENIChomozygous597136494
121469703914697040CCAAGTTCTGATTTCTGTAAAACTAAGAAGGATGTTCTCCTGCAGCAGG16GENICpossibly homozygous726491383
121469708314697084TC31GENICpossibly homozygous597136495
121470028514700286TTTGTC10GENIChomozygous726491384
121470049914700500GC8GENICpossibly homozygous598050869
121470122514701226GC17GENIChomozygous597136496
121470413214704133TTA12GENIChomozygous726491385
121470415014704151GT5GENICheterozygous598050870
121470415314704154CT7GENIChomozygous597136497