chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8104962826104962827CT28GENIChomozygous116622539
8104968235104968236TC34GENIChomozygous116622541
8104968390104968391GA32GENICpossibly homozygous116622543
8104969948104969949TC45GENICpossibly homozygous116622545
8104972943104972944AG41GENIChomozygous116622547
8104973317104973318AC53GENIChomozygous116622549
8104974485104974486TC54GENIChomozygous116622551
8104976683104976684TC57GENIChomozygous116622553
8104980178104980179CA30GENIChomozygous116622555
8104982740104982741TC51GENICpossibly homozygous116622557
8104983931104983932TC43GENICpossibly homozygous116622559
8104984890104984891CT49GENIChomozygous116622561
8104987299104987300AG57GENIChomozygous116622563
8104987567104987568GA45GENICpossibly homozygous116622565
8104988169104988170AT47GENIChomozygous116622567
8104988198104988199TA38GENIChomozygous116622569
8104988929104988930TC33GENIChomozygous116622571
8104989031104989032GT24GENICpossibly homozygous116622573
8104990238104990239TC56GENIChomozygous116622575
8104990258104990259TC54GENIChomozygous116622577