chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3117468970117468971AG29GENIChomozygous58010575
3117469144117469145CT22GENIChomozygous57620425
3117474490117474491AG34GENIChomozygous57620431
3117477818117477819A-4GENIChomozygous58178524
3117478165117478166GC16GENIChomozygous58178526
3117478469117478470AG16GENIChomozygous58178528
3117478965117478966GA28GENICpossibly homozygous57620443
3117479468117479469AATTT12GENICheterozygous58010679
3117479468117479469AATTTT12GENICheterozygous58010682
3117479468117479469AATT12GENICheterozygous58010684
3117479994117479995T-5GENICheterozygous57620447
3117480137117480138G-13GENIChomozygous58010700
3117480341117480342GA32GENICpossibly homozygous58178530
3117481245117481246CCATGT22GENICheterozygous58691759
3117481246117481258ATGTATGTATGT------------22GENICpossibly homozygous58178532
3117482688117482689CG24GENIChomozygous58010720
3117482812117482816TTGG----21GENICpossibly homozygous58010726
3117484964117484965GA15GENICheterozygous58389619
3117485923117485924TTA12GENICheterozygous58178534
3117487617117487618C-1GENIChomozygous57620457
3117488490117488491TTA10GENICheterozygous58691761
3117488491117488492A-10GENICheterozygous58010765
3117490342117490343CCT8GENIChomozygous57620461
3117487117117487119AA--15GENICheterozygous58620639
3117487118117487119A-15GENICpossibly homozygous58620640