chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
98891846288918463TC21GENIChomozygous117888002
98891851288918513GA26GENIChomozygous117888006
98891852888918529TC30GENIChomozygous117888008
98891872288918723GC41GENIChomozygous117888010
98891910388919104GA30GENIChomozygous117888012
98891911688919117GA38GENIChomozygous117888014
98891912788919128CT36GENIChomozygous117888016
98891914888919149TA38GENIChomozygous117888018
98891915088919151GA39GENIChomozygous117888020
98891916588919166AT34GENIChomozygous117888022
98891930688919307CT27GENIChomozygous117852682
98891944788919448GT32GENIChomozygous117888028
98891957888919579CA40GENIChomozygous117888030
98891990388919904TA20GENIChomozygous117888038
98891995288919953TC30GENIChomozygous117888040
98891997488919975CT26GENIChomozygous117888042
98892000888920009TC21GENIChomozygous117888044
98892024088920241TG26GENIChomozygous117888046
98892063188920632CT43GENIChomozygous117852690
98892071188920712AG35GENIChomozygous117888052