chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4133907786133907787CT10GENICpossibly homozygous56932335
4133908585133908586TTA15GENIChomozygous56932339
4133908631133908632AC11GENICpossibly homozygous56932340
4133909730133909731TC21GENICpossibly homozygous56932341
4133909885133909886AT14GENIChomozygous56932342
4133910383133910384TC26GENIChomozygous59244147
4133910573133910574GT9GENIChomozygous56932343
4133910581133910582GT12GENIChomozygous59244149
4133914627133914628GA6GENIChomozygous59244151
4133914630133914631GC6GENIChomozygous59244154
4133914705133914706TG8GENICpossibly homozygous59244156
4133914783133914784CG5GENICheterozygous59244158
4133914833133914834TTTTCC1GENIChomozygous59244160
4133914873133914874TA1GENIChomozygous59244162
4133914930133914931CT1GENIChomozygous59244164
4133914937133914938CT1GENIChomozygous59244166
4133914999133915000GA2GENICheterozygous59244170
4133915004133915005GA3GENICheterozygous59244172
4133915010133915011TC2GENIChomozygous59244174
4133915017133915018AG2GENIChomozygous59244176