chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46250696762506968CT26GENIChomozygous56918648
46250705962507060GGT17GENICpossibly homozygous56918649
46250838562508386T-13GENICheterozygous56918650
46250886762508868GGTGGCTAGA13GENIChomozygous56918651
46250909862509099AAT22GENIChomozygous56918652
46251054962510550CA24GENICpossibly homozygous56918653
46251101362511014A-14GENIChomozygous56918654
46251305962513060AT22GENIChomozygous56918655