chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
826811862681187GT17GENICpossibly homozygous631511911
826812072681208AT16GENIChomozygous631511912
826814902681491AC24GENIChomozygous631511913
826819802681981TG21GENICpossibly homozygous631511914
826827532682754TA7GENICheterozygous631511915
826837072683708CT5GENIChomozygous631511916
826838642683865CT26GENIChomozygous631511917
826839712683972TC21GENIChomozygous631511918
826840892684090TG18GENIChomozygous631511919
826848982684899TA2GENIChomozygous631511920
826850182685019CT11GENIChomozygous631511921
826855252685526AG14GENIChomozygous631511922
826863492686350T-8GENIChomozygous745682428
826864892686490CG7GENIChomozygous631511923
826884522688453T-6GENICheterozygous745682429
826893082689309TC18GENIChomozygous631511924
826902662690267CT18GENIChomozygous631511925
826905612690562CT6GENICheterozygous631511926
826913372691338T-2GENICheterozygous745682430
826916292691630TG7GENICheterozygous631511927
826917282691729TA2GENIChomozygous631511928
826918612691862AAT1GENIChomozygous745682433
826922312692232T-16GENICheterozygous745682434
826924892692490CA12GENICpossibly homozygous631511929
826932602693261GT10GENICheterozygous631511930
826936382693639G-6GENICheterozygous745682435
826941252694126C-6GENICheterozygous745682436
826944932694494CT10GENICpossibly homozygous631511931
826946482694649AAT4GENICheterozygous745682437
826956792695680GA16GENIChomozygous631511932
826970242697025CA16GENIChomozygous631511933
826976612697673TATTTATTTATT------------1GENIChomozygous745682439
826979702697971TA2GENIChomozygous631511934
826980292698030GT11GENIChomozygous631511935
827015502701551AG13GENICheterozygous631511936
827026552702656GGT10GENIChomozygous745682441
827038482703849AT13GENIChomozygous631511937
827055122705513GA20GENIChomozygous631511938
827079192707920T-2GENIChomozygous745682442
827080192708020A-11GENIChomozygous745682443
827083562708357AG15GENIChomozygous631511939
827086492708650A-4GENICheterozygous745682444
827108742710875AG19GENICpossibly homozygous631511940