chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117937113117937114GA18GENIChomozygous817937200
8117937599117937600TC21GENIChomozygous817937201
8117938840117938841CA22GENIChomozygous817937202
8117938845117938846G-22GENIChomozygous817937203
8117938987117938989TC--24GENIChomozygous817937204
8117941200117941201A-18GENIChomozygous817937205
8117945928117945930CA--18GENIChomozygous817937206
8117948034117948035TC17GENIChomozygous817937207
8117948142117948143TC14GENIChomozygous817937208
8117952745117952749AATG----11GENIChomozygous817937209
8117954073117954074CT9GENIChomozygous817937210
8117956787117956788TTTAGC9GENIChomozygous817937211
8117956795117956796CG14GENICpossibly homozygous817937212
8117960587117960588GA17GENIChomozygous817937213
8117960691117960694GGG---10GENIChomozygous817937214
8117962115117962116AG18GENIChomozygous817937215
8117962197117962198GA12GENIChomozygous817937216
8117963371117963372AG20GENIChomozygous817937217
8117963411117963412TC13GENIChomozygous817937218
8117963462117963463T-20GENIChomozygous817937219
8117963771117963772AG26GENIChomozygous817937220
8117965673117965674GC10GENIChomozygous817937221
8117968702117968703TG15GENIChomozygous817937222
8117969446117969447AG12GENIChomozygous817937223
8117969792117969793TC18GENIChomozygous817937224
8117969914117969915TTG13GENIChomozygous817937225
8117972274117972275T-19GENIChomozygous817937226