chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121725275017252751AC60GENIChomozygous115273343
121725284517252846AG50GENIChomozygous115273345
121725323017253231AC52GENICpossibly homozygous115273347
121725340617253407TG43GENIChomozygous115273349
121725343717253438TC51GENIChomozygous115273351
121725419517254196GA73GENIChomozygous115273353
121725437817254379CG61GENIChomozygous115273355
121725533317255334AG57GENIChomozygous115273357
121725674917256750GA53GENIChomozygous115273359
121725716317257164GT54GENIChomozygous115273361
121725762217257623AG42GENIChomozygous115273363
121725775617257757GA54GENIChomozygous115273365
121725834517258346AT36GENIChomozygous115273367
121725854717258548GA54GENIChomozygous115273369
121725861117258612AG42GENIChomozygous115273371
121725891117258912CT36GENIChomozygous115273373
121725519317255194AG55GENIChomozygous118246648
121725524117255242CT45GENIChomozygous118246649
121725820417258205CA13GENIChomozygous115421323
121725825517258256TC12GENIChomozygous115364970
121725882517258826TC48GENIChomozygous115364971
121725994317259944GA56GENIChomozygous115273375
121726005617260057GA51GENIChomozygous115273377
121726027017260341AACTTCCTTTTTTTTGCATGTGTGTGCATACATGAGCATTGTGTTGGATGTTGGTCCTTGGTTTCCACTGT33GENIChomozygous128966519
121725901717259029AGCTCCAGGACA49GENIChomozygous128966518
121725526017255260A45GENIChomozygous128966516
121725622817256228T53GENIChomozygous128966517
121726075917260760AG54GENIChomozygous115273379
121726169417261695GC43GENIChomozygous115273381
121726201317262014TC65GENIChomozygous115273383
121726239317262394CT58GENIChomozygous115483441