chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4220863861220863862GT10GENIChomozygous57099136
4220865688220865689GGTGTGTGTGTGTA8GENIChomozygous58374779
4220865950220865951TC24GENIChomozygous57099138
4220866163220866164AAACAGTCTC19GENIChomozygous57099139
4220866308220866309CT26GENIChomozygous57099140
4220867182220867183CT21GENIChomozygous57099141
4220867457220867458GT31GENIChomozygous57099142
4220867545220867546AT21GENIChomozygous57099143
4220870021220870022TC15GENIChomozygous57099145
4220870972220870973AATTTT9GENIChomozygous57099146
4220872787220872788TA15GENIChomozygous57099151
4220873146220873147TC31GENIChomozygous57099152
4220873722220873728ACACAC------4GENIChomozygous57099153
4220873953220873954TC40GENIChomozygous57099154
4220875508220875509CCTTT11GENIChomozygous57099155
4220875728220875729TTA21GENIChomozygous57099158
4220877048220877049GGGTGTGTGT12GENIChomozygous58374781
4220877136220877137GGTCTCTC14GENICpossibly homozygous57099160
4220877136220877137GGTCTC14GENICheterozygous58374783
4220877271220877272CG19GENICpossibly homozygous57099165
4220877449220877450CCTGTG16GENIChomozygous57099170
4220877514220877516TC--12GENIChomozygous57099172
4220877584220877586TC--13GENICheterozygous57099173
4220877696220877697GT4GENIChomozygous57367644
4220877700220877701GT4GENICheterozygous57367648
4220879291220879292GA19GENIChomozygous57099175
4220880183220880184CT18GENIChomozygous57099176
4220880485220880486GA38GENIChomozygous57099177
4220880567220880568AG35GENIChomozygous57099178
4220880591220880592AC36GENIChomozygous57099179