chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3111735654111735655CT25GENICpossibly homozygous58175565
3111735804111735805TC28GENIChomozygous57988647
3111735827111735828TG31GENICpossibly homozygous58175567
3111735906111735907TA32GENIChomozygous58175569
3111736258111736259GA19GENIChomozygous58175571
3111736750111736751CCA16GENIChomozygous57602900
3111737037111737038GA18GENIChomozygous58175573
3111737191111737192GC19GENIChomozygous57988650
3111737599111737600CCT20GENICpossibly homozygous58175575
3111737790111737791GA34GENIChomozygous58175577
3111739416111739417AG29GENIChomozygous57988655
3111739796111739797CT24GENIChomozygous58175579
3111740272111740274TC--26GENIChomozygous58175581
3111740639111740640AC21GENIChomozygous58175583
3111740640111740641TC21GENIChomozygous57988661
3111741074111741075CT19GENIChomozygous58175585
3111741114111741115CCACTT11GENIChomozygous57988664
3111741259111741260AG23GENIChomozygous57988667
3111741585111741586TC21GENIChomozygous58175587
3111741761111741762GA19GENICpossibly homozygous58175589
3111741865111741866AT17GENICpossibly homozygous58175591
3111742340111742341CT17GENIChomozygous58175595