chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117167512117167513TA26GENICpossibly homozygous54077051
7117168222117168223AG14GENICpossibly homozygous54077053
7117168417117168418TC13GENIChomozygous54077054
7117169296117169297A-14GENICpossibly homozygous54077056
7117172680117172681GA11GENICheterozygous54077060
7117173128117173129CT19GENICpossibly homozygous54077061
7117173163117173164AG13GENICheterozygous54077062
7117173640117173641G-4GENICheterozygous54077063
7117175392117175393TTG3GENICheterozygous54077065
7117177899117177900GA3GENIChomozygous54077068
7117178585117178605CAGAGATTAAATACCTTTTG--------------------5GENICheterozygous54077069
7117179373117179374TG9GENICheterozygous54077070
7117179650117179651A-8GENICheterozygous54077071
7117181489117181490TC20GENIChomozygous54077072
7117181698117181699AG12GENICpossibly homozygous54077073
7117181907117181908GA40GENIChomozygous54077074
7117182100117182101GA4GENICheterozygous54077075
7117183255117183256TG15GENIChomozygous54077079
7117183392117183393G-16GENIChomozygous54077080
7117179311117179313GA--10GENICpossibly homozygous54231375
7117179649117179651AA--8GENICheterozygous54231377