chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
38092994880929949GT35GENICheterozygous57491518
38092997280929973TTTA33GENICheterozygous57491520
38092999680929997A-24GENICheterozygous57491522
38093003880930039CT20GENICheterozygous57491524
38093011780930118AG21GENICheterozygous57491526
38093017080930171CCA33GENICheterozygous58295452
38093023880930239AG45GENICheterozygous57491528
38093034180930342AC31GENICheterozygous57491530
38093035080930351AG32GENICheterozygous57491532
38093037180930372AG36GENICheterozygous57491534
38093044180930442CCA25GENICheterozygous58295454
38093061180930612AG37GENICheterozygous57491540
38093092780930928AG39GENIChomozygous57491542
38093098680930987GA28GENICheterozygous57491544
38093107580931076GC42GENIChomozygous57491546
38093124480931245TTG32GENIChomozygous57491548
38093126580931266GGC29GENIChomozygous57491552
38093142780931428AG26GENICheterozygous58295458
38093147880931479TA32GENICheterozygous57491554
38093148180931482CT35GENICheterozygous58552564
38093153680931537AC40GENICheterozygous58295460
38093161280931613C-32GENICheterozygous58295462
38093165980931660TC42GENICheterozygous57491562
38093173980931740AG36GENICheterozygous57491564