chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105930618959306190CA18GENIChomozygous51465291
105930651759306518AC22GENIChomozygous51465293
105930651859306519TTA21GENIChomozygous51465294
105930673559306736AG26GENIChomozygous51897406
105930753859307539AG11GENIChomozygous51465298
105930782759307828CCTAG8GENICheterozygous51465299
105930782759307828CCTAA8GENICheterozygous52601092
105930782959307830CG8GENICheterozygous51465300
105930783159307832TG7GENICpossibly homozygous51465301
105930826259308263T-11GENIChomozygous51465302
105930849359308494AG8GENIChomozygous51465305
105930913659309137CT28GENIChomozygous51465307
105931002959310030CA26GENIChomozygous51465308
105931038059310381AG21GENIChomozygous51465310
105931071759310718TC14GENIChomozygous51465311
105931086859310869CT19GENIChomozygous51465312
105931155259311553CG15GENIChomozygous51465314
105931175159311752CG11GENIChomozygous51897408
105931248959312490GA15GENIChomozygous51465317
105931249259312493CA15GENIChomozygous51897410
105931292859312929TC29GENIChomozygous51465318
105931311459313115TC20GENIChomozygous51465319
105931324059313241CT21GENIChomozygous51897412
105931329859313299CT39GENIChomozygous51897414
105931348659313487G-16GENIChomozygous51897416
105931353159313532TC12GENIChomozygous51465320
105931494959314950AG17GENIChomozygous51465322
105931537659315377CA14GENIChomozygous51897418
105931537859315379CT14GENIChomozygous51897420
105931556459315565TC17GENIChomozygous51897422
105931616859316169T-16GENIChomozygous51897426
105931619859316199GA27GENIChomozygous51897428
105931626359316264GGT19GENIChomozygous51897430
105931681159316812GA18GENIChomozygous51465327
105930890959308911CG--6GENICheterozygous51662939
105931597359315974AATCTCTCTCTCTCTCTCTC3GENIChomozygous52378996
105931601459316015CCTCCTCCTCTTTT12GENIChomozygous52378998