chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108530353085303531AG19GENICpossibly homozygous116665471
108530411085304111CT5GENIChomozygous126476126
108530707785307078CG13GENIChomozygous116665475
108530758885307589TC18GENIChomozygous116665479
108530816285308163TA14GENIChomozygous116815103
108530876085308761TG14GENIChomozygous116815105
108530927685309277AG4GENIChomozygous116665481
108531005685310057TC18GENIChomozygous116665483
108531007885310079GA17GENIChomozygous116815107
108531128885311289TC14GENIChomozygous116665487
108531189885311899AC14GENIChomozygous116665489
108531269685312697AT8GENIChomozygous116665491
108531321185313212CT18GENIChomozygous116815109
108531321285313213GA18GENIChomozygous116815111
108531333185313332CT15GENIChomozygous116815113
108531351185313512CT22GENIChomozygous116665497
108531432285314323CT14GENIChomozygous116815115
108531475685314757GC10GENIChomozygous116815117
108531643185316432CT25GENIChomozygous117258190
108531774785317748AG22GENIChomozygous116665501
108531788385317884TC11GENIChomozygous116815125
108531878985318790GC4GENICheterozygous126476127
108531898485318985AT5GENIChomozygous116815127
108531937585319376CT5GENIChomozygous117258192
108532007585320076TC12GENIChomozygous116665505
108532226185322262GA24GENIChomozygous116815137
108532307185323072AG15GENIChomozygous116665509
108532486785324868TC22GENIChomozygous116665511
108532639985326400AG8GENICheterozygous118004846
108532828985328290AG20GENIChomozygous116815141
108533015885330159CT5GENIChomozygous116665513
108533133085331331CG17GENIChomozygous116665515
108533162285331623GA17GENIChomozygous116815143
108533434085334341GA9GENIChomozygous116815145
108531203285312033TG5GENICheterozygous126389055
108532594185325942AT10GENIChomozygous117018823