chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1274247446274247447CT58GENIChomozygous120513250
1274247458274247459CG57GENIChomozygous120513251
1274248132274248133GA53GENIChomozygous108654246
1274248375274248375A24GENICheterozygous130218563
1274248379274248380CA26GENICheterozygous108654248
1274249342274249343TC55GENIChomozygous108654250
1274249538274249539AG34GENIChomozygous108654252
1274253300274253301CT45GENIChomozygous120513252
1274254567274254568GA57GENIChomozygous120513253
1274254807274254808AG53GENIChomozygous108654265
1274255275274255276GA39GENIChomozygous120513254
1274257513274257514GC50GENIChomozygous108654268
1274257623274257624GA57GENIChomozygous120513255
1274258420274258421AG34GENIChomozygous108654269
1274258585274258585AAAAAT27GENIChomozygous127512852