chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8121844635121844636TC29GENIChomozygous52855910
8121845538121845539AAACACACACACACAC6GENIChomozygous53412984
8121845622121845623TC22GENIChomozygous52855914
8121845798121845799GC23GENIChomozygous52855916
8121847010121847011AG28GENIChomozygous52855918
8121847014121847015CT26GENIChomozygous52855920
8121847292121847293AAC33GENIChomozygous52855922
8121847499121847500GGAC22GENICpossibly homozygous52855928
8121848033121848043AAAAAAAAAA----------7GENICheterozygous52855932
8121848289121848290GGA13GENICpossibly homozygous52855934
8121847294121847295AAAC33GENIChomozygous53368508