chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171642944316429444GC4GENIChomozygous111296093
171642953516429536TG5GENIChomozygous111296094
171642960416429605AC6GENIChomozygous111296095
171643043416430435TC4GENIChomozygous111296096
171643046816430469AG5GENIChomozygous110970174
171643090916430910TC5GENIChomozygous111296097
171643104816431049CT6GENIChomozygous111296098
171643108216431083TG6GENIChomozygous111296099
171643127816431279TC9GENIChomozygous111296100
171643196716431968TG5GENIChomozygous111296102
171643229216432293CT7GENIChomozygous111296103
171643275016432751TC4GENIChomozygous110970180
171643302816433029TG4GENICheterozygous110970184
171643332716433328CG3GENIChomozygous110970190
171643341116433412CT8GENIChomozygous111296104
171643367516433676CT7GENIChomozygous111296105
171643465216434653TG5GENIChomozygous111296106
171643259416432595GA13GENIChomozygous111526094
171643585116435852GA3GENIChomozygous111173265
171643618316436184TG3GENIChomozygous110970194
171643718216437183GA6GENIChomozygous110970198
171643743716437438GT11GENIChomozygous111296107
171643802316438024CT13GENIChomozygous110970202
171643995116439952AG5GENIChomozygous111296108
171644015516440156AT4GENIChomozygous111173267
171644039716440398CG5GENIChomozygous111296109
171644062616440627TG10GENIChomozygous110970206
171644071916440720TG7GENIChomozygous110970208
171644152616441527CG7GENIChomozygous110970210
171644241816442419GA3GENIChomozygous111296110
171644262916442630GT2GENIChomozygous110970212