chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46250696762506968CT22GENIChomozygous666844988
46250705962507060GGT27GENICpossibly homozygous767244174
46250720462507205T-22GENIChomozygous767244175
46250838462508385AAT4GENICheterozygous767244177
46250838562508386T-4GENICheterozygous767244176
46250886762508868GGTGGCTAGA26GENIChomozygous767244178
46250909862509099AAT18GENIChomozygous767244179
46250926662509267AATG8GENICheterozygous767244182
46251054962510550CA27GENIChomozygous666844989
46251101362511014A-13GENIChomozygous767244183
46251305962513060AT27GENIChomozygous666844990