chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5126895290126895291TA28GENIChomozygous114137518
5126895299126895300TC34GENIChomozygous114137519
5126895331126895332GA26GENIChomozygous118980515
5126895515126895516CT19GENICpossibly homozygous118980516
5126895611126895612CT28GENIChomozygous114137520
5126895902126895903GA25GENIChomozygous118980517
5126896415126896416CA30GENICpossibly homozygous118980518
5126896500126896501TC24GENIChomozygous113999404
5126896521126896522TC19GENIChomozygous113999406
5126896841126896842CT25GENIChomozygous119182071
5126896847126896848TC27GENIChomozygous119182072
5126896855126896856TG25GENIChomozygous113999408
5126897109126897110CT23GENICpossibly homozygous118980519
5126897943126897944TC19GENIChomozygous113999420
5126899951126899952CG16GENIChomozygous113999428
5126900226126900227GA7GENIChomozygous113999432
5126903397126903398CA23GENICpossibly homozygous118980520
5126903426126903427CT22GENICpossibly homozygous118980521
5126906071126906072AG29GENIChomozygous113999474
5126907179126907180CT23GENICpossibly homozygous119182073
5126908245126908246GA38GENIChomozygous113999496