chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221346145221346146GA39GENIChomozygous109449393
1221347019221347020TG24GENICheterozygous108770201
1221347080221347081CT12GENICheterozygous109449394
1221347088221347089TC18GENICheterozygous109449395
1221347960221347961TC33GENIChomozygous108544497
1221348641221348642AC30GENIChomozygous109449396
1221348791221348792TG27GENIChomozygous109449397
1221349368221349369AT31GENIChomozygous108544505
1221349534221349535TG24GENIChomozygous108994737
1221349553221349554CA21GENIChomozygous108994738
1221349975221349976TC16GENIChomozygous108994739
1221350037221350038GA11GENIChomozygous109449398
1221350322221350323GA27GENIChomozygous108544511
1221351851221351852TA19GENIChomozygous108544513
1221352466221352467CT28GENIChomozygous108994742
1221352536221352537CT18GENICpossibly homozygous108994743
1221352891221352892CG13GENIChomozygous109368253
1221353357221353358GC8GENIChomozygous108544517
1221353363221353364TC7GENIChomozygous108544519
1221353539221353540AG19GENIChomozygous108544521
1221353878221353879GA18GENIChomozygous109449399
1221354080221354081GA12GENIChomozygous109449400
1221354327221354328CT18GENIChomozygous109449401
1221354727221354728AG24GENICpossibly homozygous109368256
1221354729221354730AG26GENICpossibly homozygous109368258
1221355005221355006CT22GENIChomozygous108544527
1221355320221355321GA33GENIChomozygous109449402
1221355438221355439CT23GENIChomozygous108544529
1221355597221355598TC16GENIChomozygous108544531
1221355746221355747CT41GENICheterozygous109449403
1221356006221356007TC13GENIChomozygous108544533
1221356301221356302AG12GENIChomozygous108544537
1221356316221356317AG13GENIChomozygous108544539
1221356473221356474TC11GENIChomozygous108544541
1221356941221356942GA24GENIChomozygous108994745
1221358807221358808GT12GENIChomozygous109449404
1221367933221367934GT23GENIChomozygous109449405
1221370573221370574CA36GENIChomozygous109449406