chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X127671047127671048T-7GENICheterozygous45221395
X127717776127717777TTAAGGTAC3GENIChomozygous45221493
X127717870127717871GA10GENICheterozygous45732883
X127717961127717962AAG11GENIChomozygous45221494
X127718022127718023AAG3GENICheterozygous45221495
X127718057127718058AAG1GENIChomozygous45221496
X127754022127754023CCCATGTTTACTAA9GENICheterozygous45732885
X127762633127762635GT--12GENICpossibly homozygous45221536
X127762666127762667GT18GENICpossibly homozygous45221537
X127763388127763389TC6GENICheterozygous45221541
X127788351127788352GA6GENICheterozygous45732887
X127836366127836367AAT3GENIChomozygous45221713
X127894966127894968AA--6GENICheterozygous45221821
X127907766127907767G-1GENIChomozygous45221837
X127907771127907772T-1GENIChomozygous45221838
X127907776127907777T-3GENICheterozygous45221839