chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157660034157660035GT27GENICheterozygous112906818
4157666698157666699TC27GENIChomozygous112906820
4157668604157668605TG45GENICpossibly homozygous112906822
4157668837157668838GA49GENIChomozygous112906824
4157668971157668972CG39GENIChomozygous112906826
4157669281157669282CT38GENIChomozygous112906828
4157669301157669302TA38GENIChomozygous112906830
4157669365157669366GA37GENIChomozygous112906832
4157669743157669744TC33GENIChomozygous112906834
4157669812157669813GT37GENIChomozygous112906836
4157669875157669876AG39GENIChomozygous112906838
4157670107157670108CT47GENIChomozygous112906840
4157670110157670111TC48GENIChomozygous112906842
4157670141157670142TC43GENIChomozygous112906844
4157670198157670199GA31GENIChomozygous112906846
4157670228157670229GA32GENIChomozygous112906848
4157670355157670356GT22GENICpossibly homozygous112906850
4157670656157670657CT33GENIChomozygous112906852
4157671018157671019CT29GENICpossibly homozygous112906854
4157671126157671127GA29GENICheterozygous112906856
4157671641157671642AG38GENIChomozygous112906858
4157672472157672473AG43GENIChomozygous112906860
4157672720157672721TC25GENIChomozygous112906862
4157672742157672743AG25GENIChomozygous112906864
4157672889157672890TC18GENIChomozygous112906868
4157672901157672902TC21GENIChomozygous112906870
4157672910157672911GA24GENICpossibly homozygous112906872
4157672912157672913GA24GENIChomozygous112906874
4157673005157673006CA36GENIChomozygous112906876
4157673257157673258CT25GENIChomozygous112906878
4157673392157673393CT44GENIChomozygous112906880
4157673433157673434GT37GENIChomozygous112906882
4157673536157673537CG28GENIChomozygous112906884
4157674810157674811TC33GENIChomozygous112906888
4157675212157675213GA31GENIChomozygous112906890
4157670750157670751TC33GENICheterozygous113062921