chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3117573819117573820CT26GENICpossibly homozygous58389664
3117577545117577546CCAAAT3GENIChomozygous58178653
3117577728117577729AG18GENIChomozygous58389667
3117578439117578440A-11GENICpossibly homozygous58389668
3117581122117581123CA15GENICheterozygous58389670
3117581361117581371ACACACACAC----------9GENICheterozygous58559089
3117581368117581369CG7GENICheterozygous58620670
3117583062117583063TC23GENICpossibly homozygous57620710
3117583416117583417GA11GENIChomozygous58389671
3117583538117583539CT18GENIChomozygous58389672
3117583720117583721CT7GENIChomozygous58389673
3117584542117584543CT9GENIChomozygous58389674
3117585415117585416TC23GENIChomozygous57620724
3117586314117586315TC27GENIChomozygous57620730
3117586856117586857AT18GENIChomozygous57620734