chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5142114411142114412AATG47GENICpossibly homozygous55756749
5142114412142114414CG--47GENICheterozygous55756750
5142114421142114422GA45GENICpossibly homozygous56355184
5142115423142115424CCCA19GENICpossibly homozygous55756753
5142115512142115513TTACAC21GENIChomozygous55756754
5142116406142116407GGT42GENIChomozygous55756756
5142116634142116635TA38GENIChomozygous55756757
5142116999142117000TA37GENIChomozygous55756758
5142117413142117414AC32GENIChomozygous55756759
5142118563142118564CT41GENIChomozygous55756760
5142118759142118760AG48GENIChomozygous55756761
5142118998142118999AG56GENIChomozygous55756762
5142119735142119736GA46GENIChomozygous55756763
5142120147142120148GA26GENIChomozygous55756764
5142120539142120540TC46GENIChomozygous55756765
5142120568142120569TC39GENIChomozygous55756766
5142116812142116862TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTGTGTGTG--------------------------------------------------24GENICpossibly homozygous56553473