chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105659590556595906AT17GENIChomozygous51892541
105659599156595992CA36GENIChomozygous52059414
105659630556596306GA22GENIChomozygous51892544
105659632256596323TC19GENIChomozygous51892547
105659647256596473GC16GENIChomozygous51892550
105659676356596764GA15GENIChomozygous51892553
105659718956597190TG10GENIChomozygous51656163
105659733656597337TG13GENIChomozygous51656165
105659736756597368TC18GENIChomozygous51892559
105659740556597406GA21GENIChomozygous51892562
105659764256597643TTA13GENICpossibly homozygous51892565
105659766556597666T-14GENIChomozygous51892568
105659831256598313GA13GENIChomozygous51892571
105659914456599145AT11GENIChomozygous51892574
105659937156599372AG12GENIChomozygous51892577
105659984156599842GC16GENIChomozygous51892580
105660013256600133AG17GENIChomozygous51656171
105660036756600368GA18GENIChomozygous51892583
105660079756600798TC20GENIChomozygous51892586
105660111856601119AG14GENIChomozygous51892595
105660149256601493TG12GENIChomozygous51892601
105660174556601746AG22GENIChomozygous51656181
105660197156601972GA12GENIChomozygous52059416
105660263256602633AG35GENIChomozygous51656183
105660297856602979CT25GENIChomozygous51892604
105660374456603745TC17GENIChomozygous51656185
105660450156604502CT15GENIChomozygous51892607
105660551056605517TTTTTTT-------18GENIChomozygous51892610
105660642256606423TA10GENIChomozygous51656189
105660697556606979GTGT----1GENIChomozygous52502649
105660724056607241C-3GENIChomozygous51892613
105660736456607365AG6GENIChomozygous51656193
105660771156607712TC13GENIChomozygous52059418
105660774256607743AG12GENIChomozygous51656195
105660774956607750CT13GENIChomozygous52059420