chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171642953516429536TG18GENIChomozygous111296094
171642960416429605AC19GENIChomozygous111296095
171643002516430026TC10GENIChomozygous110970170
171643043416430435TC28GENIChomozygous111296096
171643046816430469AG23GENIChomozygous110970174
171643090916430910TC21GENIChomozygous111296097
171643104816431049CT18GENIChomozygous111296098
171643108216431083TG22GENIChomozygous111296099
171643127816431279TC16GENIChomozygous111296100
171643147516431476GA25GENIChomozygous111296101
171643196716431968TG29GENICpossibly homozygous111296102
171643229216432293CT11GENIChomozygous111296103
171643275016432751TC18GENIChomozygous110970180
171643302816433029TG20GENIChomozygous110970184
171643332716433328CG22GENIChomozygous110970190
171643341116433412CT32GENIChomozygous111296104
171643367516433676CT17GENIChomozygous111296105
171643465216434653TG30GENIChomozygous111296106
171643618316436184TG14GENIChomozygous110970194
171643715416437155GA26GENIChomozygous110970196
171643718216437183GA27GENIChomozygous110970198
171643743716437438GT26GENIChomozygous111296107
171643802316438024CT33GENIChomozygous110970202
171643995116439952AG18GENIChomozygous111296108
171643418116434182CT24GENIChomozygous111173261
171643259416432595GA19GENIChomozygous111526094
171644039716440398CG34GENIChomozygous111296109
171644062616440627TG28GENIChomozygous110970206
171644071916440720TG26GENIChomozygous110970208
171644152616441527CG27GENIChomozygous110970210
171644241816442419GA12GENIChomozygous111296110
171644262916442630GT26GENIChomozygous110970212