chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3107611749107611750CCT19GENIChomozygous57963942
3107611925107611926GA10GENIChomozygous57963945
3107612095107612096GGACTA7GENIChomozygous58170131
3107612098107612099TTA6GENIChomozygous58170133
3107612101107612102TTGC7GENICpossibly homozygous58170135
3107612102107612103TTTTTTA6GENIChomozygous58170137
3107612530107612531T-16GENIChomozygous57963948
3107613484107613486TG--16GENICpossibly homozygous58170139
3107614230107614231TC7GENIChomozygous57963954
3107618057107618058AG21GENIChomozygous57963957