chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
38092994880929949GT27GENIChomozygous57491518
38092997280929973TTTA25GENIChomozygous57491520
38092999680929997A-21GENIChomozygous57491522
38093003880930039CT22GENIChomozygous57491524
38093011780930118AG27GENIChomozygous57491526
38093023880930239AG23GENIChomozygous57491528
38093034180930342AC24GENIChomozygous57491530
38093035080930351AG24GENIChomozygous57491532
38093037180930372AG23GENIChomozygous57491534
38093044180930442CCAAAAAAAAA9GENICheterozygous57491536
38093051480930515GA17GENIChomozygous57491538
38093061180930612AG17GENIChomozygous57491540
38093092780930928AG24GENIChomozygous57491542
38093098680930987GA19GENIChomozygous57491544
38093107580931076GC14GENIChomozygous57491546
38093124480931245TTG21GENIChomozygous57491548
38093125980931260GA21GENIChomozygous57491550
38093126580931266GGC20GENIChomozygous57491552
38093147880931479TA28GENIChomozygous57491554
38093149180931492AT26GENIChomozygous57491556
38093161380931614CT19GENIChomozygous57491558
38093162580931626GA17GENIChomozygous57491560
38093165980931660TC24GENIChomozygous57491562
38093173980931740AG24GENIChomozygous57491564
38093180580931806AG25GENIChomozygous57491566
38093187980931880GA25GENIChomozygous57491568
38093188180931882CT24GENIChomozygous57491570
38093044180930442CCAAAAAAAA9GENICheterozygous58688506
38093148180931482CT28GENIChomozygous58552564