chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108774650287746503CT21GENICheterozygous52072661
108774651387746514GA26GENICheterozygous51532717
108774652287746523CT26GENICheterozygous51532718
108774654587746546GT24GENICheterozygous51532719
108774658587746586AC27GENICheterozygous52205128
108774662487746625CA24GENICheterozygous52205130
108774675587746756TA20GENICheterozygous51532721
108774675987746760TG18GENICheterozygous51532722
108774676387746764CT19GENICheterozygous51532723
108774677187746772TC16GENICheterozygous51728339
108774678287746783AG14GENICheterozygous51532724
108774679187746792TC13GENICheterozygous51532725
108774687287746873TC11GENICheterozygous51532731
108774687787746878AC12GENICheterozygous53531442
108774707487747075GT39GENICheterozygous51532733
108774709987747100C-39GENICheterozygous52393259
108774710087747101AT39GENICheterozygous53531443
108774710287747103AAG40GENICheterozygous52393261
108774719687747197CA16GENICheterozygous51532734
108774723287747233GC23GENICheterozygous51532735
108774893687748937TC23GENICheterozygous51532740
108774900087749001TC27GENICheterozygous51532741
108774906587749066CT19GENICheterozygous51532742
108774912587749126TG20GENICheterozygous51532744
108774917587749176GA16GENICheterozygous51532746
108774704987747050GA27GENICheterozygous52164379