chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1274247446274247447CT50GENIChomozygous120513250
1274247458274247459CG56GENIChomozygous120513251
1274248132274248133GA46GENIChomozygous108654246
1274248375274248375A20GENICheterozygous130218563
1274248379274248380CA21GENICheterozygous108654248
1274249342274249343TC59GENIChomozygous108654250
1274249538274249539AG37GENIChomozygous108654252
1274253300274253301CT52GENIChomozygous120513252
1274254567274254568GA61GENIChomozygous120513253
1274254807274254808AG40GENIChomozygous108654265
1274255275274255276GA56GENIChomozygous120513254
1274257513274257514GC66GENIChomozygous108654268
1274257623274257624GA63GENIChomozygous120513255
1274258420274258421AG42GENIChomozygous108654269
1274258585274258585AAAAAT38GENIChomozygous127512852