chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
25404907254049073TC29GENIChomozygous58826567
25405034054050341CCA6GENIChomozygous58826570
25405117254051173TC35GENIChomozygous58826571
25405332354053324G-31GENIChomozygous58826572
25405411054054114AAAA----13GENIChomozygous58826573
25405504754055048CCT27GENIChomozygous58826574
25405518954055190GA30GENIChomozygous58826575
25405588054055881A-21GENIChomozygous58826576
25405647354056474AG30GENIChomozygous58826577
25405738754057388GT26GENIChomozygous58826578
25405755654057557AG26GENIChomozygous58826579
25405822954058230AAACACACAC6GENICheterozygous58826580
25405822954058230AAACACACACACAC6GENICheterozygous60750548
25406012554060126AAGGCAG29GENICheterozygous60539625
25406013354060134GA27GENICpossibly homozygous58826581
25406058454060585C-17GENIChomozygous58826582
25406059054060591GA18GENIChomozygous58826583
25406070854060709GA24GENIChomozygous58826584
25406108154061082GGGGTGTGGT13GENIChomozygous58826585
25406108354061085CA--14GENIChomozygous58826586
25406108954061090TTGGA11GENIChomozygous58826587
25406109154061092TTAGG10GENIChomozygous58826588
25406346854063469TC34GENIChomozygous58826589
25406443154064432GA36GENIChomozygous58826590
25406445354064454CT29GENIChomozygous58826591
25406473954064740GA20GENIChomozygous58826592
25406481654064817CCTCTT5GENICheterozygous61114096
25406607054066071TC31GENICpossibly homozygous58826598
25405332454053325GA31GENIChomozygous60443865
25406481654064817CCTCT5GENICheterozygous60480273