chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1226035651226035652TA52GENIChomozygous134796152
1226038452226038453AG47GENIChomozygous108997523
1226039900226039901CG38GENIChomozygous134796153
1226040372226040373GA61GENIChomozygous134796154
1226042634226042635TC25GENIChomozygous108558480
1226042729226042730CG30GENIChomozygous108558481
1226043575226043576GA47GENIChomozygous108558483
1226039899226039899TG22GENICpossibly homozygous134780399
1226043870226043870TG31GENIChomozygous134780400
1226045484226045485GT67GENIChomozygous134796155
1226045995226045996CT55GENIChomozygous134796156
1226046364226046365AG45GENIChomozygous108558490
1226047316226047317GA44GENIChomozygous108558493
1226048306226048307C24GENIChomozygous134780401
1226048445226048445TTTCTTTTT29GENICpossibly homozygous127488006
1226048519226048520AG33GENIChomozygous108997548
1226048560226048561AG45GENIChomozygous108997549