chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3114219255114219256TC32GENIChomozygous111678488
3114220255114220256CT15GENIChomozygous111678489
3114221077114221078CT28GENIChomozygous112140014
3114223074114223075AG21GENIChomozygous111678490
3114223634114223635TC16GENIChomozygous111678491
3114223670114223671AG5GENIChomozygous111678492
3114224219114224220GT16GENIChomozygous112140015
3114224482114224483TC20GENIChomozygous111678494
3114225556114225557TC14GENIChomozygous112140016
3114225996114225997AG4GENIChomozygous112010063
3114227148114227149TC18GENIChomozygous112140017
3114227271114227272GA19GENIChomozygous112140018
3114229070114229071CT22GENIChomozygous112140019
3114229100114229101TC20GENIChomozygous111678496
3114229101114229102GA19GENICpossibly homozygous112140020
3114230221114230222CT16GENIChomozygous112140021
3114230233114230234CT20GENIChomozygous112140022
3114231605114231606TC24GENIChomozygous111678499
3114231870114231871AG8GENIChomozygous111678500
3114232185114232186TC12GENIChomozygous112255828
3114232291114232292TC7GENIChomozygous111678501
3114232376114232377GC8GENIChomozygous125832267
3114234303114234304GA10GENIChomozygous125865559
3114234637114234638AG6GENIChomozygous112140024
3114235582114235583AG8GENIChomozygous112010077
3114236206114236207GA15GENIChomozygous112140025
3114236701114236702AG11GENIChomozygous112140026
3114237306114237307CG26GENIChomozygous112140027