chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1203542986203542987CT27GENIChomozygous135791214
1203543104203543105TC27GENIChomozygous135791215
1203543873203543874CT28GENIChomozygous135791216
1203543984203543985G27GENIChomozygous402979263
1203543984203543985GT27GENICheterozygous402979264
1203543987203543988GT27GENIChomozygous135791217
1203544797203544798CT21GENIChomozygous135791218
1203545998203545999AG34GENIChomozygous135791219
1203546110203546111AG27GENIChomozygous135791220
1203547890203547891AG33GENIChomozygous135791222
1203549001203549002CT31GENIChomozygous135791223
1203552161203552162AG34GENIChomozygous135791225
1203555649203555650GC23GENIChomozygous135791230
1203555060203555061CA21GENIChomozygous144260814
1203546046203546046A31GENIChomozygous135455535
1203559368203559369CT23GENIChomozygous144260815
1203560353203560354AG19GENIChomozygous144260816
1203556585203556585ACA20GENIChomozygous144231288
1203560517203560518TA9GENIChomozygous153906427
1203560856203560857GA15GENIChomozygous144260817
1203561064203561068ATCC24GENIChomozygous135455538
1203561202203561203CA23GENIChomozygous144260818
1203561211203561212TC24GENIChomozygous135791235
1203561401203561402CT24GENIChomozygous144260819
1203561539203561540CT26GENIChomozygous144260820
1203561915203561916AG23GENIChomozygous144260821