chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5142114411142114412AATG3GENIChomozygous55756749
5142114421142114422GA1GENIChomozygous56355184
5142116406142116407GGT22GENIChomozygous55756756
5142116634142116635TA17GENIChomozygous55756757
5142116999142117000TA20GENICpossibly homozygous55756758
5142117413142117414AC28GENICpossibly homozygous55756759
5142118563142118564CT16GENICpossibly homozygous55756760
5142118759142118760AG21GENIChomozygous55756761
5142118998142118999AG28GENIChomozygous55756762
5142119735142119736GA22GENICpossibly homozygous55756763
5142120147142120148GA19GENICpossibly homozygous55756764
5142120539142120540TC16GENIChomozygous55756765
5142120568142120569TC19GENIChomozygous55756766