chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3170354258170354259CT25GENICpossibly homozygous111834318
3170356262170356263AT30GENIChomozygous111834320
3170356401170356402AT41GENIChomozygous111834322
3170356511170356512CT3GENIChomozygous111834324
3170357958170357959GA66GENIChomozygous111834326
3170358050170358051TG56GENIChomozygous111834328
3170358205170358206CT55GENIChomozygous111834330
3170358303170358304GT47GENICpossibly homozygous111834332
3170358311170358312GA43GENIChomozygous111834334
3170358743170358744TC52GENIChomozygous111834336
3170359093170359094GA44GENICpossibly homozygous111834338
3170359350170359351CT49GENIChomozygous111834340
3170360663170360664CA46GENIChomozygous111834342
3170360792170360793GC47GENIChomozygous111834344
3170361906170361907GT21GENICpossibly homozygous111834346
3170362065170362066AG49GENIChomozygous111834348
3170362161170362162GA60GENIChomozygous111834350
3170363076170363077GA50GENIChomozygous111834352