chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4152502401152502402TC72GENICheterozygous56986210
4152502404152502405CT72GENICheterozygous57842908
4152502450152502451GT37GENICheterozygous57349540
4152502453152502454AT34GENICheterozygous57349542
4152502462152502463AG39GENICheterozygous57349544
4152502463152502464AG38GENICheterozygous57349546
4152502474152502475AG39GENICheterozygous57349548
4152502476152502477AG41GENICheterozygous57349550
4152502512152502513GA58GENICheterozygous57349554
4152502521152502522CA64GENICheterozygous57842909
4152503069152503070GT93GENICheterozygous58160306
4152504514152504515A-2GENICheterozygous56986212
4152506598152506599GT26GENICheterozygous56986213
4152506605152506606GC30GENICheterozygous56986214
4152506663152506664CCA21GENIChomozygous56986215
4152506692152506693TA27GENIChomozygous56986216
4152506723152506724GGTT26GENIChomozygous56986217
4152506867152506868TC50GENIChomozygous56986218
4152506962152506963AG42GENIChomozygous56986219
4152507171152507172GT53GENIChomozygous56986220