chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117724816117724817CT18GENIChomozygous54749650
7117724920117724921GA35GENIChomozygous54749652
7117725028117725029GA21GENIChomozygous54749654
7117725372117725375TTT---12GENIChomozygous54231551
7117726760117726761T-15GENICheterozygous54749656
7117727882117727883G-22GENICpossibly homozygous54749658
7117730343117730344T-16GENICheterozygous54078464
7117730939117730940TTTGTG24GENICpossibly homozygous54078466
7117731616117731617CCTTTTTTT14GENICheterozygous55030311
7117734108117734109GA39GENIChomozygous54749660
7117735481117735482CCGT27GENICpossibly homozygous54078478
7117743782117743783AG27GENIChomozygous54078492