chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5147803989147803991CC62GENICpossibly homozygous128253962
5147805155147805156TC55GENIChomozygous114047380
5147805333147805334AC55GENIChomozygous114047382
5147805352147805352A60GENIChomozygous128253963
5147805356147805357A62GENIChomozygous128253964
5147805500147805501G59GENIChomozygous128253965
5147805883147805884GA65GENIChomozygous114047384
5147806880147806880A57GENICpossibly homozygous128253966
5147807611147807612TC56GENIChomozygous114047386
5147809187147809188AG54GENIChomozygous114047388
5147809230147809231TC33GENIChomozygous122415376
5147809815147809816CG27GENIChomozygous114047390
5147810036147810037AT70GENIChomozygous114047392
5147810064147810067CTC62GENIChomozygous128253968
5147810187147810188TG46GENICpossibly homozygous114047394
5147810259147810260TG48GENIChomozygous114047396
5147810358147810359GA59GENIChomozygous114047398
5147810632147810633A33GENICheterozygous128253969
5147811709147811710TC81GENIChomozygous114047408
5147811735147811736TC73GENIChomozygous114047410
5147812098147812099CG71GENIChomozygous114153118
5147811930147811931CT74GENIChomozygous114153116
5147811962147811963GA62GENIChomozygous114153117