chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3114218778114218779CT17GENIChomozygous112140012
3114219255114219256TC20GENIChomozygous111678488
3114220255114220256CT20GENIChomozygous111678489
3114221077114221078CT23GENIChomozygous112140014
3114223074114223075AG28GENIChomozygous111678490
3114223634114223635TC27GENIChomozygous111678491
3114224219114224220GT15GENIChomozygous112140015
3114225556114225557TC28GENIChomozygous112140016
3114227148114227149TC15GENIChomozygous112140017
3114227271114227272GA21GENIChomozygous112140018
3114229070114229071CT29GENIChomozygous112140019
3114229100114229101TC25GENIChomozygous111678496
3114229101114229102GA25GENIChomozygous112140020
3114230221114230222CT29GENIChomozygous112140021
3114230233114230234CT27GENIChomozygous112140022
3114231605114231606TC21GENICpossibly homozygous111678499
3114231870114231871AG17GENIChomozygous111678500
3114235582114235583AG17GENIChomozygous112010077
3114236206114236207GA17GENIChomozygous112140025
3114236701114236702AG17GENIChomozygous112140026
3114237306114237307CG27GENIChomozygous112140027