chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4161446528161446529GA48GENIChomozygous71276356
4161446855161446856CG51GENIChomozygous71276358
4161446863161446864CT47GENICpossibly homozygous71276360
4161448461161448462CT17GENICpossibly homozygous71276362
4161448698161448699TC68GENICheterozygous71276366
4161449928161449929CT70GENIChomozygous71276388
4161450430161450431TC71GENIChomozygous71276390
4161450642161450643AC50GENIChomozygous71276392
4161450915161450916AG41GENIChomozygous71276394
4161451267161451268CT38GENIChomozygous71276396
4161451824161451825AG66GENIChomozygous71276398
4161452668161452669CT67GENIChomozygous71276400
4161452791161452792TC41GENIChomozygous71276402
4161453638161453639TC39GENIChomozygous71276404
4161453675161453676CT46GENIChomozygous71276406
4161454044161454045AG14GENIChomozygous71276408
4161454108161454109TC8GENIChomozygous71276410
4161454481161454482TC33GENIChomozygous71276412
4161454956161454957GA44GENIChomozygous71276413
4161455267161455268GA26GENIChomozygous71276415
4161455883161455884TC53GENIChomozygous71276417
4161456037161456038CG43GENICheterozygous71276425
4161456045161456046CG44GENICheterozygous71276427
4161456782161456783GA44GENIChomozygous71276429
4161457019161457020GA48GENIChomozygous71276431
4161457528161457529CT34GENIChomozygous71276433
4161459693161459694CT63GENIChomozygous71276435
4161460513161460514TC48GENICpossibly homozygous71276437
4161460619161460620CT79GENIChomozygous71276439
4161463155161463156TG21GENIChomozygous71276441
4161463525161463526AG70GENIChomozygous71276443