chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214124348214124349AG19GENIChomozygous792549082
1214127012214127013GA28GENICheterozygous792549083
1214127053214127054GA26GENICpossibly homozygous792549084
1214127433214127434TC30GENIChomozygous792549085
1214129031214129032TC34GENIChomozygous792549086
1214130226214130227GA35GENIChomozygous792549087
1214131357214131358AG46GENIChomozygous792549088
1214132380214132381AG38GENIChomozygous792549089
1214132530214132531CT38GENIChomozygous792549090
1214137707214137708CG34GENICheterozygous792549091
1214138871214138872GA49GENIChomozygous792549092
1214140632214140633CT29GENIChomozygous792549093
1214140827214140828GT35GENIChomozygous792549094
1214140994214140995GT32GENIChomozygous792549095
1214141343214141344AG41GENIChomozygous792549096
1214143187214143188CT30GENIChomozygous792549097
1214143347214143348AG30GENIChomozygous792549098
1214144102214144103GA35GENIChomozygous792549099
1214146027214146028TC28GENIChomozygous792549100
1214147016214147017CT23GENIChomozygous792549101