chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
67925343679253437TC9INTERGENIChomozygous55168160
67925344879253449GA9INTERGENIChomozygous55168161
67925347479253475CCGG4INTERGENIChomozygous55168162
67925367979253682TTT---3INTERGENIChomozygous55168163
67925378479253785TC3INTERGENICheterozygous55718313
67925401679254017TG3INTERGENICheterozygous55168164
67925404479254045AG12INTERGENIChomozygous55168165
67925406679254067GA12INTERGENICpossibly homozygous55168166
67925410279254103GA19INTERGENIChomozygous55168167
67925419279254193AAGACCTGGAGAAATG2INTERGENICheterozygous54528089
67925455779254558GT14INTERGENIChomozygous54906658
67925471879254719TC15INTERGENIChomozygous55168168
67925476979254770AATC4INTERGENIChomozygous55168169
67925481679254817GT10INTERGENIChomozygous55168170
67925486879254869AG4INTERGENIChomozygous55168171
67925513979255140GT8INTERGENIChomozygous55168172
67925551179255512TC20INTERGENICpossibly homozygous55168173
67925560579255606GA7INTERGENIChomozygous55168174
67925561679255617TC7INTERGENIChomozygous55168175
67925580779255808TC6INTERGENICheterozygous54528091
67925606779256068CA13INTERGENICheterozygous55168176
67925635179256352AT14INTERGENIChomozygous55168177
67925663179256632TC15INTERGENIChomozygous55168178
67925684679256847TC16INTERGENICpossibly homozygous55168179
67925722079257221TG10INTERGENICpossibly homozygous55168180
67925725979257260CA9INTERGENICpossibly homozygous55168181
67925755579257556GT6INTERGENIChomozygous55168182
67925786079257864TATC----1INTERGENIChomozygous55168184
67925791379257914GGTT2INTERGENIChomozygous55168185
67925795579257956CA4INTERGENIChomozygous55168186