chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130117240130117241CA17GENIChomozygous54110353
7130118246130118247T-15GENIChomozygous54110354
7130118274130118275CA19GENIChomozygous54110355
7130120300130120301AG16GENIChomozygous54110356
7130120410130120411CCTT11GENICheterozygous54110358
7130120484130120485GC16GENIChomozygous54110359
7130120642130120643TC28GENIChomozygous54110360
7130121330130121331AG30GENIChomozygous54110361
7130121351130121352CCAGGCCTGATTCAG28GENIChomozygous54110362
7130121574130121575CT33GENIChomozygous54110363
7130121716130121717AG24GENIChomozygous54110364
7130121749130121750AG29GENIChomozygous54110365
7130121879130121905GAGAGAGAGAGAGAGAGAGAGAGAGG--------------------------16GENICheterozygous55031074
7130121881130121905GAGAGAGAGAGAGAGAGAGAGAGG------------------------16GENICpossibly homozygous55010362
7130124264130124265TC26GENIChomozygous54110366
7130124636130124637GA24GENIChomozygous54110367