chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
115882244258822443GA3GENICheterozygous126319403
115894737458947375GA12GENIChomozygous126278346
115895623358956234GT23GENIChomozygous126278348
115896389558963896AG6GENIChomozygous126278350
115896391958963920CA4GENIChomozygous115973996
115896627558966276CA4GENIChomozygous126319404
115897470658974707GA3GENICheterozygous126319405
115897471258974713GA8GENICheterozygous126319406
115897992158979922TG22GENIChomozygous126278352
115897995158979952CG18GENIChomozygous126278354
115897997158979972TC7GENIChomozygous126286457
115898005058980051CA6GENIChomozygous126286458
115898005558980056TA9GENIChomozygous126278356
115898006558980066TA13GENIChomozygous126278358
115904822459048225GT6GENIChomozygous126296819
115904822759048228CA7GENIChomozygous126296820
115904825859048259CA12GENIChomozygous126286459
115908679259086793GC19GENIChomozygous115875884
115910373859103739GT6GENICheterozygous126302471
115910374459103745GT5GENICheterozygous126302473
115913720959137210TA3GENICheterozygous126319407
115917082259170823TA4GENIChomozygous126319408
115918810459188105GT4GENICheterozygous126319409
115925499259254993CA9GENIChomozygous126278364
115929730259297303GC24GENIChomozygous126278366
115929746259297463TG17GENIChomozygous126278368
115929752859297529GT33GENIChomozygous126278370
115930649959306500AG7GENIChomozygous126296826
115936825759368258AC6GENIChomozygous126278372
115937013659370137CA6GENIChomozygous126278374
115937583759375838CT7GENIChomozygous126278378