chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4152502401152502402TC57GENICheterozygous56986210
4152502404152502405CT57GENICheterozygous57842908
4152502450152502451GT19GENICheterozygous57349540
4152502462152502463AG18GENICheterozygous57349544
4152502463152502464AG17GENICheterozygous57349546
4152502512152502513GA38GENICheterozygous57349554
4152502521152502522CA44GENICheterozygous57842909
4152503011152503012GA80GENICheterozygous57842910
4152503049152503050GC96GENICheterozygous57842911
4152504514152504515A-4GENICheterozygous56986212
4152506598152506599GT13GENICheterozygous56986213
4152506605152506606GC13GENICheterozygous56986214
4152506663152506664CCA3GENIChomozygous56986215
4152506692152506693TA5GENIChomozygous56986216
4152506723152506724GGTT5GENIChomozygous56986217
4152506867152506868TC21GENIChomozygous56986218
4152506962152506963AG27GENIChomozygous56986219
4152507171152507172GT20GENIChomozygous56986220
4152503069152503070GT88GENICheterozygous58160306