chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
49851481998514820CT38GENIChomozygous112794265
49851490098514901AG35GENIChomozygous112794267
49851504498515045AG47GENIChomozygous112794269
49851508998515090GA43GENIChomozygous112794271
49851512998515130GA34GENIChomozygous112794273
49851518398515184AG34GENIChomozygous112794275
49851594698515947CG23GENIChomozygous112794277
49851596398515964CT21GENIChomozygous112794279
49851603398516034TC37GENIChomozygous112794281
49851622898516229CA21GENIChomozygous112794283
49851627898516279GA20GENIChomozygous112794285
49851630198516302AG26GENIChomozygous112794287
49851632098516321CA26GENIChomozygous112794289
49851650898516509GA24GENIChomozygous112794291
49851668698516687CT33GENIChomozygous112794293
49851670798516708CT36GENIChomozygous112794295
49851700798517008AT11GENIChomozygous112794297
49851709798517098AT12GENIChomozygous112794299
49851721198517212CT13GENIChomozygous112794301
49851724198517242TG11GENIChomozygous112794303
49851771998517720GA36GENIChomozygous112794304
49851772198517722GA36GENIChomozygous112794306
49851792398517924GT16GENIChomozygous112794308
49851802598518026GT22GENIChomozygous112794310
49851827598518276TA33GENIChomozygous112794312
49851828898518289CT34GENIChomozygous112794314
49851862998518630AG48GENIChomozygous112794316
49851863898518639AG48GENIChomozygous112794318