chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3109816430109816431GC42GENIChomozygous141529363
3109818826109818827CT35GENIChomozygous141529364
3109820292109820293CT28GENIChomozygous141529365
3109820884109820885CT56GENIChomozygous141529366
3109823498109823499AG30GENIChomozygous141529367
3109823502109823503AG30GENIChomozygous141529368
3109823645109823646TC52GENIChomozygous141529369
3109824586109824587TC54GENIChomozygous141529370
3109818972109818974TG39GENIChomozygous136583637
3109824084109824094TCTCTGTCTC28GENIChomozygous141479408
3109824979109824980AG48GENIChomozygous141529371