chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4135405340135405341GA60GENICheterozygous60098388
4135405348135405349TC60GENICheterozygous60043431
4135405390135405391TC60GENICheterozygous60043433
4135405421135405422CT39GENICheterozygous60200804
4135405424135405425GT39GENICheterozygous60182231
4135405434135405435TC38GENICheterozygous60200806
4135406596135406597CT78GENICheterozygous56937470
4135406608135406609AC83GENICheterozygous60043443
4135406689135406690CT98GENICheterozygous56937472
4135406698135406699CT96GENICheterozygous56937473
4135406735135406736AT84GENICheterozygous56937474
4135407563135407564TG78GENICheterozygous56937495
4135407589135407590CA101GENICheterozygous56937496
4135407613135407614CG117GENICheterozygous56937497
4135407644135407645GA130GENICheterozygous56937498
4135407737135407738TG115GENICheterozygous60182233
4135407738135407739CT114GENICheterozygous60182235
4135407742135407743TC111GENICheterozygous60182237
4135407747135407748AC111GENICheterozygous56937501
4135407748135407749AC111GENICheterozygous56937502
4135407755135407756GT116GENICheterozygous56937503
4135407757135407758TC118GENICheterozygous56937504
4135407877135407878CA95GENICheterozygous57336977
4135407908135407909GA86GENICheterozygous56937505
4135408282135408283CT31GENICheterozygous57836651