chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
202802729928027300TA14GENIChomozygous109248232
202802738128027382CT19GENIChomozygous109373461
202802743628027437AT21GENIChomozygous109373463
202802749028027491AG23GENIChomozygous109154764
202802824428028245AG14GENIChomozygous109154766
202802923228029233GA13GENIChomozygous109248234
202803156228031563GA22GENIChomozygous109310316
202803244628032447CT25GENIChomozygous109248236
202803261328032614TC29GENIChomozygous109154774
202803822828038229GA18GENIChomozygous109154788
202805150928051510AG16GENIChomozygous109248238
202805251128052512TC9GENICheterozygous109154796
202805403828054039AG20GENIChomozygous109154804
202805482528054826AG30GENIChomozygous109154808
202805523328055234AT16GENIChomozygous109154810
202805538528055386GA18GENIChomozygous109248240
202805757928057580CT23GENIChomozygous109248242
202805801928058020TC41GENIChomozygous109154818
202805828128058282CA29GENIChomozygous109154820
202806153428061535CG25GENIChomozygous109154826
202806638428066385TC32GENIChomozygous109154836
202806668828066689AG22GENIChomozygous109154838
202806842828068429CT25GENIChomozygous109248246
202806868928068690TG18GENIChomozygous109248248
202807061028070611CA22GENIChomozygous109154846
202807184928071850CT14GENIChomozygous109248250
202807268428072685TC31GENIChomozygous109154852
202807295328072954AG36GENIChomozygous109154854
202807496628074967TC30GENIChomozygous109154864
202807620128076202AG9GENIChomozygous109154868
202807630828076309GA14GENIChomozygous109154870