chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2117990633117990634CA17GENICpossibly homozygous624123086
2117991497117991498CT6GENIChomozygous624123087
2117994890117994891TC12GENICheterozygous624123088
2117995042117995043T-9GENIChomozygous740435315
2117996552117996553AG8GENICpossibly homozygous624123089
2117996858117996859CT12GENIChomozygous624123090
2117997021117997022GT3GENICheterozygous624123091
2117997039117997040GT1GENIChomozygous624123092
2117997043117997044CA1GENIChomozygous624123093
2117997044117997045TC1GENIChomozygous624123094
2117997053117997054CG1GENIChomozygous624123095
2117997066117997067C-1GENIChomozygous740435316
2117997079117997080C-4GENIChomozygous740435317
2117998083117998084CT2GENIChomozygous624123096
2117998167117998170TTT---1GENIChomozygous740435318
2117998262117998263CA5GENICheterozygous624123097
2117998342117998343AG4GENICheterozygous624123098
2117998363117998364AG1GENIChomozygous624123099
2117998368117998369TG1GENIChomozygous624123100
2117998377117998378AG1GENIChomozygous624123101
2117998380117998381AG1GENIChomozygous624123102
2117998383117998384TG1GENIChomozygous624123103
2117998444117998445A-11GENIChomozygous740435321
2117998533117998534GA9GENIChomozygous624123104
2117998771117998772GA19GENICpossibly homozygous624123105
2117998949117998950AC19GENICpossibly homozygous624123106
2117998975117998976TA13GENICheterozygous624123107
2117998994117998995TC20GENIChomozygous624123108
2117999795117999796AG6GENICheterozygous624123109
2117999887117999888TG13GENICpossibly homozygous624123110
2118000372118000373T-2GENIChomozygous740435322
2118000476118000477AG4GENIChomozygous624123111
2118001569118001570CT18GENIChomozygous624123112
2118001690118001691CG19GENIChomozygous624123113
2118001805118001806CG20GENICpossibly homozygous624123114
2118002630118002631AG8GENICheterozygous624123115
2118003105118003106CT12GENIChomozygous624123116
2118004282118004283GA14GENICpossibly homozygous624123117
2118005992118005993CT24GENIChomozygous624123118