chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7135495578135495579TC30GENIChomozygous54131382
7135497598135497599CT41GENIChomozygous54131387
7135497604135497605CT42GENIChomozygous54131388
7135497606135497607TTA41GENIChomozygous54131389
7135497609135497610CCT43GENIChomozygous54131390
7135497629135497630CT48GENIChomozygous54131391
7135497632135497633TTA49GENIChomozygous54131392
7135497639135497640GGC48GENIChomozygous54131393
7135497678135497679CG40GENIChomozygous54131394
7135497700135497701CT39GENIChomozygous54131395
7135497954135497955CT32GENIChomozygous54131396
7135498481135498482C-25GENIChomozygous54131397
7135498541135498542GA28GENIChomozygous54131398
7135499073135499074CT29GENIChomozygous54131399
7135499459135499460GA16GENIChomozygous54131400
7135499511135499516GGGTC-----13GENICheterozygous55031613
7135500177135500178TC32GENIChomozygous54131401
7135500819135500820A-20GENIChomozygous54252509
7135501051135501052CT28GENIChomozygous54131402
7135501092135501093TC34GENIChomozygous54131403
7135502790135502791TA26GENIChomozygous54131404
7135504091135504092TC27GENIChomozygous54131405
7135504433135504434TTACAC11GENICheterozygous54131406
7135504433135504434TTAC11GENICheterozygous54252513
7135504872135504873C-12GENICheterozygous54131407
7135505112135505113CA7GENIChomozygous54252515
7135505126135505127CT9GENIChomozygous54131409
7135505872135505873TG25GENIChomozygous54131410
7135506076135506077CT33GENIChomozygous54131411
7135503541135503542A-24GENIChomozygous54923353