chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
25096645250966453CCTGAG16GENIChomozygous59689468
25096652150966522TTAC6GENICheterozygous59689470
25096656750966568TG10GENIChomozygous58817783
25096692050966921CA18GENIChomozygous59689472
25096738350967384GA26GENIChomozygous58817784
25096888650968887GA14GENIChomozygous59689474
25096916450969165CT14GENIChomozygous59689476
25096978450969785AG12GENIChomozygous58817791
25096991650969917AG27GENIChomozygous58817792
25097006850970069G-13GENIChomozygous58817793
25097078650970787T-7GENICpossibly homozygous58817796
25097101850971019G-23GENIChomozygous58817797
25097159450971595GA18GENIChomozygous59689478
25097164250971643TC12GENIChomozygous59689480
25097235650972357GGT17GENIChomozygous58817800
25097396950973970AAGAGGGAGG4GENIChomozygous58817806
25097399050973991GT5GENIChomozygous59689482
25097399850974000GA--3GENIChomozygous58817808
25097418550974186G-13GENIChomozygous59689484
25097422550974226AG14GENIChomozygous58817809
25097438250974383G-22GENIChomozygous59689486
25096951550969516CCACACACACACACA17GENICheterozygous60479533