chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
114907462349074624CT27GENIChomozygous51355422
114907487649074877TC28GENICpossibly homozygous51355424
114907512749075128CT25GENIChomozygous51355426
114907575749075758GA27GENIChomozygous51355428
114907696149076962GT27GENIChomozygous51355430
114907764349077644GA21GENIChomozygous51355432
114907805949078060AG27GENIChomozygous51355434
114908000449080005AG24GENIChomozygous51355436
114908059649080597GGCA17GENIChomozygous51355438
114908060249080604GC--18GENIChomozygous51355440
114908110949081110A-17GENIChomozygous51270695
114908140249081403AG37GENICpossibly homozygous51355442
114908328749083288AG17GENIChomozygous51355444
114908371149083712GA37GENIChomozygous51355446
114908499649084997TTG5GENIChomozygous51355448
114908662049086622AC--7GENIChomozygous51270696
114908668649086687TC11GENIChomozygous51355450
114908716049087161GA22GENICpossibly homozygous51355452
114908719649087197GA23GENICpossibly homozygous51355454
114908749049087491CT23GENIChomozygous51355456
114908804949088050GA17GENIChomozygous51355458
114909021449090215CT29GENIChomozygous51355460
114909033949090340GA27GENIChomozygous51355462
114908786249087863GGACACCTTCC28GENIChomozygous50774329