chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214124348214124349AG11GENIChomozygous801735184
1214124410214124411CA11GENIChomozygous801735185
1214126166214126167TA39GENICheterozygous801735186
1214127053214127054GA36GENICheterozygous801735187
1214127433214127434TC34GENICpossibly homozygous801735188
1214129031214129032TC33GENIChomozygous801735189
1214130226214130227GA36GENIChomozygous801735190
1214131357214131358AG21GENIChomozygous801735191
1214132380214132381AG21GENIChomozygous801735192
1214132530214132531CT19GENIChomozygous801735193
1214138871214138872GA24GENIChomozygous801735194
1214140632214140633CT29GENIChomozygous801735195
1214140827214140828GT37GENIChomozygous801735196
1214140994214140995GT24GENIChomozygous801735197
1214141343214141344AG25GENIChomozygous801735198
1214143187214143188CT19GENIChomozygous801735199
1214143347214143348AG26GENIChomozygous801735200
1214144102214144103GA14GENIChomozygous801735201
1214146027214146028TC22GENIChomozygous801735202
1214147016214147017CT29GENIChomozygous801735203