chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4142142327142142328TC21GENICpossibly homozygous57504026
4142143652142143653CT18GENICpossibly homozygous57504028
4142144024142144025GT20GENICpossibly homozygous57504030
4142144725142144726AG15GENIChomozygous57504032
4142145014142145015GA7GENIChomozygous57504034
4142145387142145388GA18GENICpossibly homozygous57504036
4142147057142147058AG16GENICheterozygous57504038
4142150037142150040GAG---9GENIChomozygous57504044
4142150348142150349CA17GENIChomozygous57504046
4142150852142150853CA16GENICpossibly homozygous57504048
4142151037142151038AC15GENIChomozygous57504050
4142152675142152676TC9GENICpossibly homozygous57504052
4142154785142154786GC7GENIChomozygous57504054
4142155900142155901CT17GENIChomozygous57504056
4142155943142155944CT20GENIChomozygous57504058
4142157157142157158TTC4GENIChomozygous56960107
4142157175142157176CCA7GENIChomozygous56960108
4142157742142157743CCT4GENICheterozygous57504062
4142157831142157832TTA19GENICpossibly homozygous57504064
4142158503142158504GGT8GENICheterozygous57504066
4142158878142158879AT17GENICpossibly homozygous57504068
4142159366142159367AG14GENIChomozygous57504070