chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4162612755162612756GT12GENIChomozygous58177475
4162613467162613468AG34GENIChomozygous57004686
4162613652162613653GA34GENICpossibly homozygous57004687
4162613653162613654CA35GENICpossibly homozygous57004688
4162614485162614486GA27GENIChomozygous57004689
4162614498162614499CCG32GENIChomozygous57004690
4162614499162614500AAGG28GENIChomozygous57004692
4162614525162614526AG24GENIChomozygous57004693
4162615093162615094GA22GENIChomozygous57004695
4162615824162615826TT--15GENIChomozygous57546233
4162615853162615854TTTTTG17GENICheterozygous57004697
4162615942162615943TC20GENIChomozygous57004698
4162616434162616435AG29GENIChomozygous57004699