chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3114218778114218779CT25GENIChomozygous112140012
3114219255114219256TC18GENIChomozygous111678488
3114219755114219756CT5GENIChomozygous112140013
3114220255114220256CT29GENIChomozygous111678489
3114221077114221078CT27GENIChomozygous112140014
3114223074114223075AG19GENIChomozygous111678490
3114223634114223635TC25GENIChomozygous111678491
3114223670114223671AG23GENIChomozygous111678492
3114224219114224220GT35GENIChomozygous112140015
3114224482114224483TC15GENIChomozygous111678494
3114225556114225557TC21GENIChomozygous112140016
3114225996114225997AG30GENIChomozygous112010063
3114227148114227149TC18GENIChomozygous112140017
3114227271114227272GA30GENIChomozygous112140018
3114229070114229071CT25GENIChomozygous112140019
3114229100114229101TC17GENIChomozygous111678496
3114229101114229102GA17GENIChomozygous112140020
3114230221114230222CT30GENIChomozygous112140021
3114230233114230234CT31GENIChomozygous112140022
3114231605114231606TC14GENIChomozygous111678499
3114231870114231871AG22GENIChomozygous111678500
3114233647114233648TC24GENICpossibly homozygous112140023
3114233751114233752CG29GENIChomozygous111678502
3114234051114234052TC34GENICheterozygous111678504
3114234637114234638AG21GENIChomozygous112140024
3114235582114235583AG25GENIChomozygous112010077
3114236206114236207GA20GENIChomozygous112140025
3114236701114236702AG16GENIChomozygous112140026
3114237306114237307CG33GENIChomozygous112140027