chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4208845925208845926GGT32GENIChomozygous57067241
4208846156208846157GGGTGTGT25GENICpossibly homozygous57067242
4208848127208848128TC41GENIChomozygous57067245
4208848897208848898AATGTTT28GENIChomozygous57067246
4208848902208848903AT36GENIChomozygous57067247
4208849302208849303GA30GENIChomozygous57067248
4208850160208850161CCATT25GENIChomozygous57067249
4208850346208850347GT25GENIChomozygous57067251
4208850677208850678GGAC20GENIChomozygous57067254
4208850504208850505TC22GENIChomozygous57067252
4208850622208850623AG30GENIChomozygous57067253
4208851020208851021AC35GENIChomozygous57067255
4208851230208851236TGTGTA------19GENICpossibly homozygous57067256
4208851337208851338CT23GENIChomozygous57067258
4208851338208851339CG23GENIChomozygous57067259
4208851391208851392GGAC28GENIChomozygous57067260
4208851636208851637A-23GENIChomozygous57067261
4208851850208851851TC26GENIChomozygous57067262
4208851899208851900CT27GENIChomozygous57067263
4208852108208852109AG25GENIChomozygous57067264
4208852330208852331CG15GENIChomozygous57067265