chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117561589075615891AAC9GENICpossibly homozygous50832580
117561983475619835AG17GENIChomozygous50963753
117561984675619847CCA19GENIChomozygous50963754
117561987575619876AC15GENIChomozygous50963755
117562025675620257TG26GENIChomozygous50963756
117562052275620523AG36GENIChomozygous50963757
117562083675620837AG24GENIChomozygous50963758
117562104675621048AA--12GENICheterozygous50963759
117562104775621048A-12GENICheterozygous51243606
117562139875621400CC--8GENIChomozygous51169825
117562141775621418AACAC19GENIChomozygous51169826
117562141875621419TTCACACACACTCAC19GENIChomozygous51169827
117562149475621496CG--18GENICheterozygous50832582
117562150275621548CACACACACACACTCACACACACACACACTCACACACACACACACT----------------------------------------------22GENICheterozygous51169828