chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10109972573109972574AAGTGTGTGT3GENIChomozygous51600694
10109972864109972865GGTTTT3GENICheterozygous51600695
10109972864109972865GGTT3GENICheterozygous52085308
10109972904109972905AG27GENIChomozygous51600696
10109973184109973185AG32GENIChomozygous51600697
10109973262109973263TA32GENIChomozygous51600698
10109973347109973348TC27GENIChomozygous51600699
10109973540109973541GA24GENIChomozygous51600700
10109974875109974880GTGTG-----28GENIChomozygous51600701
10109975491109975503ACACACACACAC------------5GENIChomozygous51600702
10109975533109975545AGAGAAAGAGAG------------15GENIChomozygous51600703
10109976102109976103GA35GENIChomozygous51600704
10109976247109976248GC27GENICpossibly homozygous51600705
10109976371109976372G-27GENICheterozygous51600706
10109976375109976376GT33GENICpossibly homozygous51600707
10109976380109976387TTGTTTG-------27GENICheterozygous51600708
10109976383109976391TTTGTTTG--------6GENIChomozygous51600709
10109976639109976640TC37GENIChomozygous51600710
10109976655109976656CT36GENIChomozygous51600711
10109976941109976942GA46GENIChomozygous51600712
10109977040109977044CACA----29GENIChomozygous51600713
10109977064109977065CT36GENIChomozygous51600714
10109977462109977463GA40GENIChomozygous51600715
10109977776109977777CT28GENIChomozygous51600716
10109978463109978464GA32GENIChomozygous51600717
10109978962109978963CCA22GENIChomozygous51600718
10109979045109979046AG16GENIChomozygous51600719
10109979053109979054GGAACCC15GENIChomozygous51600720