chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7135495578135495579TC20GENIChomozygous54131382
7135497598135497599CT28GENIChomozygous54131387
7135497604135497605CT27GENIChomozygous54131388
7135497606135497607TTA27GENIChomozygous54131389
7135497609135497610CCT27GENIChomozygous54131390
7135497629135497630CT33GENIChomozygous54131391
7135497632135497633TTA33GENIChomozygous54131392
7135497639135497640GGC32GENIChomozygous54131393
7135497678135497679CG27GENIChomozygous54131394
7135497700135497701CT23GENIChomozygous54131395
7135497954135497955CT21GENIChomozygous54131396
7135498481135498482C-18GENIChomozygous54131397
7135498541135498542GA24GENIChomozygous54131398
7135499073135499074CT26GENIChomozygous54131399
7135499459135499460GA11GENIChomozygous54131400
7135499511135499516GGGTC-----8GENICheterozygous55031613
7135500177135500178TC34GENIChomozygous54131401
7135500819135500820A-21GENIChomozygous54252509
7135501051135501052CT26GENIChomozygous54131402
7135501092135501093TC22GENIChomozygous54131403
7135502790135502791TA16GENIChomozygous54131404
7135503540135503542AA--20GENICheterozygous55031615
7135504091135504092TC21GENIChomozygous54131405
7135504433135504434TTACAC10GENIChomozygous54131406
7135505112135505113CA2GENIChomozygous54252515
7135505126135505127CT8GENIChomozygous54131409
7135505872135505873TG20GENIChomozygous54131410
7135506076135506077CT21GENIChomozygous54131411
7135503541135503542A-20GENICpossibly homozygous54923353