chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
826811862681187GT16GENIChomozygous590408068
826812072681208AT12GENICpossibly homozygous590408069
826814902681491AC20GENIChomozygous590408070
826819802681981TG12GENICpossibly homozygous590408071
826837072683708CT2GENIChomozygous590408072
826838642683865CT13GENIChomozygous590408073
826839712683972TC15GENIChomozygous590408074
826840892684090TG15GENIChomozygous590408075
826850182685019CT9GENIChomozygous590408076
826855252685526AG11GENIChomozygous590408077
826863492686350T-6GENIChomozygous724083018
826864892686490CG3GENIChomozygous590408078
826893082689309TC7GENIChomozygous590408079
826902662690267CT11GENICheterozygous590408080
826905612690562CT4GENIChomozygous590408081
826913372691338T-1GENIChomozygous724083019
826914072691408GA2GENIChomozygous590408082
826916292691630TG4GENICheterozygous591758662
826917282691729TA5GENIChomozygous591758663
826922312692232T-9GENICheterozygous724083022
826924892692490CA6GENICheterozygous591758664
826932602693261GT9GENICheterozygous590408083
826933122693313TC3GENICheterozygous590408084
826936382693639G-4GENICheterozygous724083023
826941252694126C-4GENIChomozygous724083024
826944932694494CT6GENIChomozygous591758665
826946482694649AAT1GENIChomozygous724083025
826956792695680GA12GENICheterozygous591758666
826970242697025CA16GENIChomozygous591758667
826976612697673TATTTATTTATT------------1GENIChomozygous724083027
826979702697971TA4GENIChomozygous590408085
826980292698030GT14GENICheterozygous590408086
827015502701551AG17GENICheterozygous590408087
827026552702656GGT5GENIChomozygous724083029
827038482703849AT5GENICheterozygous590408088
827055122705513GA14GENIChomozygous590408089
827079192707920T-2GENICheterozygous724083030
827080192708020A-10GENIChomozygous724083031
827083562708357AG6GENIChomozygous590408090
827108742710875AG15GENICpossibly homozygous590408091