chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117167512117167513TA22GENIChomozygous54077051
7117168222117168223AG15GENIChomozygous54077053
7117168417117168418TC11GENIChomozygous54077054
7117168951117168952AG18GENIChomozygous54077055
7117169296117169297A-13GENIChomozygous54077056
7117169552117169553TC12GENIChomozygous54077058
7117172680117172681GA20GENIChomozygous54077060
7117173128117173129CT12GENIChomozygous54077061
7117173163117173164AG14GENIChomozygous54077062
7117173640117173641G-3GENIChomozygous54077063
7117175389117175390GT24GENIChomozygous54077064
7117175392117175393TTG25GENIChomozygous54077065
7117176591117176593AA--9GENICheterozygous54077066
7117176592117176593A-9GENICheterozygous54077067
7117177899117177900GA24GENIChomozygous54077068
7117178585117178605CAGAGATTAAATACCTTTTG--------------------19GENIChomozygous54077069
7117179311117179313GA--21GENIChomozygous54231375
7117179373117179374TG20GENIChomozygous54077070
7117179649117179651AA--18GENICheterozygous54231377
7117179650117179651A-18GENICheterozygous54077071
7117181489117181490TC28GENIChomozygous54077072
7117181698117181699AG21GENIChomozygous54077073
7117181907117181908GA20GENIChomozygous54077074
7117182100117182101GA16GENIChomozygous54077075
7117183039117183040GGTGTA6GENICheterozygous54077077
7117183039117183040GGTA6GENICheterozygous54077078
7117183255117183256TG24GENIChomozygous54077079
7117183392117183393G-27GENIChomozygous54077080
7117173420117173448TGTGTGTGTGTGTGTGTGTGTGTGTGTG----------------------------5GENIChomozygous55000172
7117180789117180790CCCTCTCTCTCT3GENIChomozygous55000174