chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71107022711070228TC6GENIChomozygous53787298
71107044511070446TA9GENIChomozygous53787303
71107061011070611CT13GENIChomozygous53787304
71107073011070731GC11GENIChomozygous53787305
71107093211070944AAAAAAAAAAAA------------9GENIChomozygous53787306
71107106511071066GA10GENIChomozygous53787307
71107117911071180GGAGATTTAGCTCAGTGGT1GENIChomozygous54954276
71107123011071231GGAA4GENIChomozygous53787310
71107136811071369AT15GENIChomozygous53787311
71107139511071396GA17GENIChomozygous53787312
71107190211071903TC9GENIChomozygous53787313
71107190611071907AG8GENIChomozygous53787314
71107204711072048AG15GENIChomozygous53787315
71107224511072246GA7GENIChomozygous53787316
71107239811072399AG5GENIChomozygous53787317
71107242811072429CG10GENIChomozygous53787318
71107242911072430AG10GENIChomozygous53787319
71107252511072526CT4GENIChomozygous53787320
71107275611072758AC--5GENIChomozygous53787328
71107295911072960AC1GENIChomozygous53787338
71107305611073057GA1GENIChomozygous53787339
71107307011073071AAC1GENIChomozygous53787340
71107319511073196TC3GENIChomozygous53787341
71107324011073241AG7GENIChomozygous53787342
71107328511073286CT7GENIChomozygous53787343
71107330311073304AG6GENIChomozygous53787344
71107372311073724CG10GENICheterozygous53787354
71107375311073754TC8GENIChomozygous53787355
71107396711073968CT10GENIChomozygous53787357
71107323911073240GA7GENIChomozygous54710171