chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1274938724274938725TTG8GENICpossibly homozygous685190253
1274938740274938741GT15GENICheterozygous510517397
1274938754274938755GT16GENICpossibly homozygous510517398
1274939101274939102GA65GENIChomozygous507238522
1274939138274939139TA61GENIChomozygous507238523
1274939157274939158AG65GENIChomozygous507238524
1274939651274939652CT74GENIChomozygous507238525
1274939719274939720AT92GENICpossibly homozygous507238526
1274939810274939811TG60GENIChomozygous507238527
1274939870274939871AG43GENIChomozygous507238528
1274939926274939929GGG---27GENICheterozygous685190254
1274939935274939936TC40GENICheterozygous507238529
1274941986274941987GA96GENICheterozygous510517399
1274941989274941990CT101GENICheterozygous510517400
1274942018274942019GA128GENICheterozygous507238530
1274942061274942062GA127GENICheterozygous507238531
1274942071274942072AG129GENICheterozygous507238532
1274942092274942093GA116GENICheterozygous510517401
1274942118274942119TG97GENICheterozygous510517402
1274942135274942136TTG74GENICheterozygous685190255