chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105930651759306518AC46GENIChomozygous51465293
105930651859306519TTA45GENIChomozygous51465294
105930826259308263T-16GENIChomozygous51465302
105930849359308494AG18GENIChomozygous51465305
105930903859309039GA24GENIChomozygous51465306
105930913659309137CT25GENIChomozygous51465307
105931002959310030CA32GENICpossibly homozygous51465308
105931038059310381AG32GENIChomozygous51465310
105931071759310718TC31GENIChomozygous51465311
105931086859310869CT29GENIChomozygous51465312
105931155259311553CG10GENIChomozygous51465314
105931192459311925CT19GENICpossibly homozygous51465316
105931248959312490GA36GENIChomozygous51465317
105931292859312929TC33GENIChomozygous51465318
105931311459313115TC31GENIChomozygous51465319
105931353159313532TC28GENIChomozygous51465320
105931455759314558GA27GENIChomozygous51465321
105931494959314950AG26GENIChomozygous51465322
105931556459315565TC34GENICpossibly homozygous51897422
105931601459316015CCTCCTCCTCTTCT12GENIChomozygous52460838
105930836659308367AT10GENIChomozygous51662937
105930886759308868AAACACAC5GENIChomozygous52460836
105931172159311722TTACACAC8GENIChomozygous52460837
105932013959320140GA31GENIChomozygous52062161
105931724259317243C-26GENIChomozygous52062159