chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101656656216566563CA8GENICheterozygous818257178
101656660616566607GA8GENICheterozygous818257179
101656664216566643AG10GENICheterozygous818257180
101656706416567065CT21GENICheterozygous818257181
101656720016567201TC16GENICheterozygous818257182
101656756216567563GA13GENICheterozygous818257183
101656761616567617T-15GENICheterozygous818257184
101656780116567802AG12GENICheterozygous818257185
101656811216568113TC19GENICheterozygous818257186
101656820616568207TTA11GENICheterozygous818257187
101656828316568284CG14GENICheterozygous818257188
101656831216568313TTA13GENICheterozygous818257189
101656857116568572TC32GENICheterozygous818257190
101656861516568616CT20GENICheterozygous818257191
101656900616569007CG27GENICheterozygous818257192
101656932216569323CG17GENICheterozygous818257193
101656934916569350CG17GENICheterozygous818257194
101656937816569379TC17GENICheterozygous818257195
101656972116569722TC16GENICheterozygous818257196
101656975416569755CT19GENICheterozygous818257197
101656981016569811TG12GENICheterozygous818257198
101657047516570476CT18GENICheterozygous818257199
101657109116571092GA24GENICheterozygous818257200
101657138116571382CT13GENICheterozygous818257201
101657157116571572CG13GENICheterozygous818257202
101657160916571610AG11GENICheterozygous818257203
101657302916573030CT7GENICheterozygous818257204
101657357416573575AT17GENICheterozygous818257205
101657421616574217GT19GENICheterozygous818257206
101657439416574395GA16GENICheterozygous818257207
101657444816574449CT13GENICheterozygous818257208
101657475516574756GA15GENICheterozygous818257209
101657514416575145TC12GENIChomozygous818257210
101657532216575331GTCCTTCCA---------14GENICheterozygous818257211
101657540116575402AATT8GENIChomozygous818257212
101657561316575614AC14GENIChomozygous818257213
101657571616575717TTA13GENIChomozygous818257214
101657583916575865ACACACACACACACACACACACACAC--------------------------10GENICheterozygous818257215
101657653716576538GGT17GENIChomozygous818257216