chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2187611815187611816CT28GENICpossibly homozygous110167564
2187612300187612301AG24GENIChomozygous110167566
2187613004187613005GA28GENICpossibly homozygous111343834
2187614464187614465AG25GENIChomozygous110167567
2187615132187615133GT19GENIChomozygous111343838
2187616518187616519TC19GENIChomozygous110167569
2187618414187618415AT32GENIChomozygous110167570
2187621037187621038TC40GENICpossibly homozygous110167571
2187621410187621411CT26GENIChomozygous111343840
2187621956187621957CT28GENICpossibly homozygous110167573
2187622246187622247AC13GENIChomozygous110167574